Novel deletion alleles carrying CYP21A1P/A2chimeric genes in Brazilian patients with 21-hydroxylase deficiency

Congenital adrenal hyperplasia (CAH) is an autosomal recessive inborn error of metabolism due to the deficiency of one of the enzymes involved in the adrenal steroidogenesis [1]. More than 95% of the cases are due to deficiency of 21-hydroxylase enzyme (21-OHD; OMIM +201910). Diminished or absent 21-hydroxylase activity leads to reduction or abolishment of cortisol and aldosterone syntheses, consequently, an over production of androgens occurs [1, 2]. Different clinical presentations are classified in classical form that can be salt-wasting (SW) or simple-virilizing (SV), and late-onset non-classical (NC) form [1–3]. Mutations on CYP21A2 gene, which encodes the enzyme, are responsible for the disease [2, 3].

The CYP21A2 gene and CYP21A1P, its pseudogene, are located within the class III locus of the human major histocompatibility complex at the short arm of chromosome 6 [4, 5]. Both have 10 exons, except that CYP21A1P is inactive due to deleterious mutations [6, 7]. Approximately 30 kb separate CYP21A2 from CYP21A1P. The genes of the fourth component of complement C4A and C4B, also map to this locus and are located, respectively, upstream and downstream to the CYP21A1P [4, 5].

In addition other genes, such as RP1 and TNXB and their truncated gene fragments or pseudogenes, RP2 and TNXA, are present within this genetic unit [8]. Each RP, C4, CYP21, TNX copy together forms the RCCX module [8] that maps within approximately 30 kb [9–11]. In general, 70% of alleles are bimodular (two RCCX units) in most populations [12]. Nevertheless, monomodular (16%), and trimodular (14%) alleles with long and short C4B gene variants are not uncommon [12].

Deletion or duplication of CYP21A1P or CYP21A2 together with C4A or C4B always occurs [8, 13–15]. The deletion and large gene conversion were the first mutations described in 21-hydroxylase deficiency alleles [16–19]. Generally, disease-causing 30-kb deletions extend from 3'end CYP21A1P and include C4B and 5' end CYP21A2 to form inactive CYP21A1P/A2 chimeric genes [20–27]. Whereas monomodular alleles with C4A/C4B chimeric genes may also be formed after unequal crossovers, they are frequently associated to a functional CYP21A2 gene copy [13, 22]. Such rearrangements can be recognized in Southern blots using Taq I restriction enzyme where C4 and CYP21 chimeric genes produce 6.4- and 3.2-kb fragments, respectively [22, 23]. Deletions, large gene conversions and duplications may be evaluated either by Southern blot [3] or by the recently developed Multiplex Ligation-dependent Probe Amplification (MLPA) technique [24]. As CYP21A1P/A2 chimeric genes may carry different pseudogene-derived mutations, disease-causing deletion alleles may vary according the chimeric gene composition [21, 22, 25, 26]. Novel CYP21A1P/A2 chimeric genes have been continuously described in different studies [27, 28].

In Brazil, 30-kb deletion monomodular alleles correspond to ~9% of disease-causing alleles [29, 30]. The present study describes the variability of such alleles in Brazilian patients (n = 20) with 21-hydroxylase deficiency using the conventional Southern blot, ASO-PCR and sequencing techniques combined to recently developed MLPA technique. Nine different and two novel monomodular haplotypes are reported. A 6.4-kb Taq I fragment corresponding to a C4B/C4A chimeric gene was unusually associated to CYP21A1P/A2 chimeric gene that also bore novel and rare single nucleotide polymorphisms (SNPs). Another allele was identified with a CYP21A1P/A2 gene carrying both p.P34L and p.H62L mutations in exon 1, however p.P30L, the most frequent pseudogene-derived mutation in this exon, was absent. The study of 59 healthy controls revealed that the novel p.P34L mutation is not pseudogene-derived and occurred only in alleles carrying the 30-kb deletion whereas the rare p.H62L mutation can be pseudogene-derived since it was found in 3.4% pseudogene sequences.

Southern blot analysis with CYP21 and C4 probes was performed to distinguish deletions from large gene conversions. ASO-PCRs using CL6N or CL6M sequences as selective primers were performed to investigate both pseudogene-derived mutation and polymorphisms present in chimeric CYP21A1/A2 and CYP21A2 genes. All family members have been analyzed; therefore, pseudogenes and chimeric genes carrying CL6M sequences could be distinguished. Southern blot revealed 30-kb deletion in 20 patients with different genotypes (table 2; Figure 2).

MLPA technique was used to confirm Southern blot results and to obtain data on the composition of chimeric genes since it includes one probe for each C4A and C4B genes, and three and five probes, respectively, for CYP21A1P and CYP21A2 genes (Figure 1b). The MLPA kit available also analyzes TNXB located within the RCCX locus and CREBL1 on chromosome 6p21.3 and nineteen control genes as well. For all patients, normalized data showed two copies for TNXB and CREBL1 genes (Figure 3) on chromosome 6 and also for control genes (data not shown) indicating no copy number variation in other loci.

Patients 1 and 2, who were children of consanguineous marriages, were homozygous for a monomodular allele. However, hybridization results with C4 probe indicated a 6.4-kb Taq I fragment in patient 2, whereas patient 1 presented the usual 7.0-kb C4A fragment (Figure 2a). Molecular investigation on patient's 2 family demonstrated that the novel allele has been transmitted through three generations (data not shown). MLPA indicated similar composition of CYP21A1P/A2 chimeric genes in both cases (Figure 3a, upper panel), but once again the two patients differed in the C4 gene composition (Figure 3a, lower panels). Patient 2, who carried the 6.4-kb Taq I fragment, presented MLPA signal for two copies only for C4A probe, whereas patient 1, who carried the 7.0-kb C4A Taq I fragment, showed signals for two copies of C4A and C4B probes, suggesting that both C4 in the genotype have exon 19 sequences corresponding to C4B gene. Therefore, the two different C4 sequence compositions indicate distinct 30-kb deletion alleles. Patient 1 showed haplotype II (table 3) that, besides the C4A/B chimeric copy, also presented the C allelic variant at both -4 (SNP-rs6470) and g.395 (SNP-rs6462) nucleotides. Haplotype I is unique for patient 2 (table 3). In addition to the C4B/A^[6.4] gene, it carries the novel -289T > C SNP in CYP21A1P/A2 promoter region. The T variant at g.395 (SNP-rs6462) nucleotide and the rare pseudogene-derived g.1253A variant (SNP-rs28691121) were also detected (table 3).

Patients 3 and 4 presented Southern blot results compatible with compound heterozygosis for 30-kb deletion and large gene conversion in which no signal for 3.7-kb CYP21A2 fragment was observed, whereas C4A ^[7.0] and C4B ^[6.0] fragments were present with intensities of 2:1 (Figure 2b). In MLPA experiments C4A:C4B ratios for patients 3 and 4 were 2:1 and 1:2, respectively (Figure 3b, upper panel). Both showed MLPA profiles compatible with mono-/bimodular compound heterozygosis with two different CYP21A1P/A2 chimeric genes (Figure 3b). However, the composition of monomodular allele in each case could only be defined after MLPA analysis of their parents (data not shown). For patient 3, the breakpoint between exon 3 and 4 in the chimeric CYP21A1P/A2 gene was defined for the paternal inherited monomodular allele. The maternal inherited bimodular allele carrying large gene conversion presented a complete pseudogene sequence indicated by the 2:1 ratio for probes CYP21A1P-3'end and CYP21A2-exon 8 in MLPA (Figure 3b, left lower panel) instead of the 1:2 expected if it was a chimeric gene with CYP21A2-3'end. Similar results were obtained for patient 4 except that in this case the complete pseudogene was concluded to be associated to the monomodular allele, whereas the chimeric CYP21A1P/A2 gene with recombination breakpoint between exon 3 and 4 was associated to the bimodular allele with large gene conversion (Figure 3b, right lower panel). In addition, based on MLPA analysis of her parents (data not shown), the maternal bimodular allele in patient 4 demonstrated to carry one of C4 copies in which C4A probe could not hybridize; therefore the 1:3 ratio observed in her mother indicated absence of C4A exon 17 sequences and presence of C4B exon 19 sequences which is suggestive of a chimeric C4A/B gene or a gene conversion at exon 17 (Figure 3b, right lower panel). Considering C4 composition and CYP21A1P/A2 SNPs, the 30-kb deleted alleles in patients 3 and 4 correspond to haplotypes V and III, respectively (table 3). Haplotype V is defined by the presence of the novel p.P34L and the rare p.H62L mutations, but absence of the pseudogene-derived p.P30L, in exon 1. The variant -308G and the variant C at -4 and g.395 nucleotides characterized this haplotype in which the recombination breakpoint was located between exon 3 and 4.

For other sixteen patients (5-20) who were compound heterozygous with monomodular and bi-, tri- or a probable tetramodular alleles bearing pseudogene-derived mutations in the CYP21A2 gene (Figure 2c-e; table 2), different C4A to C4B and CYP21A1P to CYP21A2 probe ratios in MLPA were observed (Figure 3c-g). These patients were divided in two major groups according to the status of exon 6 in the CYP21A1P/A2 chimeric genes: patients 5-8 with mutant exon 6 are shown in Figure 3c, and patients 9-20 with normal exon 6 in Figure 3d-g.

Chimeric CYP21A1P/A2 gene composition for alleles in patients 5-7 seemed to be similar to that in patients 1 and 2 with mutant exon 6 and normal exon 8 (Figure 3a-c, upper panels). However, C4A:C4B ratios were 2:3, suggesting that both C4A copies may carry exon 19 corresponding to C4B gene similar to that observed for patient 1. MLPA results for each family (data not shown) indicated the segregation of both C4 and CYP21 chimeric genes in the same allele (Figure 3c, left lower panel). Patient 8 presented 2:1 MLPA ratio for C4A:C4B sequences in agreement with Southern blotting. MLPA showed that 21-hydroxylase gene copy in this case corresponded to a complete pseudogene as the ratio for probes CYP21A1P 3'-end and CYP21A2-exon 8 was 2:1 as described above for patients 3 and 4 (Figure 3c, right lower panel). SNPs in chimeric genes classified the monomodular alleles in patients 5-7 within haplotype II (table 3). Besides deletion, duplication and chimeric gene composition, MLPA analyzes could identify compound heterozygosis for p.I172N in patient 7 (table 2; Figure 3c), because the probe used for CYP21A2 exon 4 anneals to the normal sequence at codon 172. Patient 8 showed haplotype IV, which can be differentiated from III at the SNPs g.1645G > C (SNP-rs6472; p.S268T) and at the g.2110C>T (p.R356W) mutation (table 3).

MLPA results for patients 9-20 were shown in Figure 3d-g. Additionally, the probable localization of recombination breakpoint within CYP21A1P/A2 chimeric genes divided them in two groups: patients 9-17 with breakpoint between exon 3 and 4 (Figure 3d-f) and patients 18-20 between exon 1 and intron 2 (Figure 3g). A combination of mono- and a probable tetramodular allele was considered for patient 9 after analysis of allelic segregation in the family (Figure 2e). This was the most probable combination to explain the relative intensity for C4A ^[7.0]:C4B ^[6.0] (2:3) and for CYP21A2 ^[3.7]:CYP21A1P ^[3.2] (1:4) fragments in the patient. The mother presented ratios of 2:1 for C4A ^[7.0]:C4B ^[5.4] and 1:3 for CYP21A2 ^[3.7]:CYP21A1P ^[3.2] and was positive for p.P30L, IVS2-13A/C > G and Δ8 mutations in ASO-PCR experiments indicating a deleted allele with CL6N sequence. The daughter inherited the 30-kb deleted allele from the mother, therefore she should carry an allele with three copies of each C4B and CYP21A1P to produce the relative intensities observed in the Southern blot (Figure 2e, lanes 2 and 3). Patients 10 and 11 were compound heterozygotes for tri- and monomodular alleles. These genotypes may explain the 2:2 ratio for C4A and C4B genes observed in Southern blot (Figure 2d). However, a 2:2 ratio for C4A:C4B in MLPA experiments has been observed only for patient 11. Patient 10 showed a 2:3 gene ratio, which is probably due to a positive hybridization signal for exon 19 C4B probe within the C4A gene copy in the paternal trimodular allele, deduced from the family analysis, therefore his most probable genotype is shown in Figure 3d (middle panel). An additional difficulty in interpreting MLPA results for patient 10 was that he also carried p.Q318X in CYP21A2 gene copy of the paternal inherited trimodular allele indicated in ASO-PCR experiments (table 2). As CYP21A2 exon 8 MLPA probe anneals to the normal sequence at codon 318, the result expected in this case was a ratio of 2:1 for probes CYP21A1P 3'UTR to CYP21A2 exon 8, if both pseudogenes in the trimodular allele were mutant in codon 318. However a ratio 2:3 was obtained. Analysis of his parents (data not shown) indicated that the two pseudogenes in the paternal trimodular allele might carry the normal sequence in codon 318 (Figure 3d, middle panel). The monomodular alleles carried by patients 10 and 11 were classified, respectively, within haplotype V and VI (table 3).

Patients 12-14 presented 2:2 MLPA ratios for C4A:C4B contrasting with the 2:1 obtained on Southern blot (Figure 2c). In these cases, familial analysis demonstrated that the bimodular alleles they carry in compound heterozygosis with monomodular alleles, probably, contain C4A genes formed by 5'-end C4A ^[7.0], C4A exon 17, but exon 19 corresponds to C4B specific sequences (Figure 3e). The monomodular allele in patient 12 corresponds to haplotype VI, whereas patients 13 and 14 carry haplotype VII (table 3). Haplotype VI differs from VII by the -449A>G (SNP-rs28361032) and g.395T > C (SNP-rs6462).

Patients 15-19 demonstrated C4A:C4B ratios of 2:1 in both Southern blotting and MLPA (Figure 3f-g). A 3:0 ratio in MLPA for C4A:C4B was observed for patient 20, whereas Southern blotting showed a ratio of 2:1. This result might indicate a C4A gene copy with a 6.0-kb Taq I fragment in which exon 17 sequences correspond to C4A and C4B specific sequences at exon 19 are absent, therefore the most probable genotype in this case is shown in Figure 3g (right lower panel). MLPA indicated compound heterozygosis for p.I172N in patients 17 and 19 (table 2; Figure 3f,g). Likewise, it also detected compound heterozygosis with p.Q318X mutation in patient 18 (table 2; Figure 3g). The recombination breakpoint indicated in MLPA for patients 15-17 was between exon 3 - 4 (Figure 3f). Sequencing data indicated haplotype V for alleles in patients 15 and 16 and haplotype VII for patient 17 (table 3). The recombination breakpoint indicated in MLPA for patients 18-20 was between exon 1 and intron 2 (Figure 3f-g). However, sequencing results suggested distinct alleles within this group. In haplotype VIII, which is shared by patients 18 and 19, the recombination breakpoint was probably located between the SNP 560_566insG and 602A > C (SNP-rs6451) as shown in table 3. Whereas, the recombination breakpoint for the allele carried by patient 20 (table 3, haplotype IX) was probably located at the beginning of intron 2 since it carried the variant A at the g.419 position (SNP - rs6448), which is more frequent in CYP21A2 gene and the nucleotide C at 547 position that is characteristic of the CYP21A2 gene.

Sequencing 170 CYP21A2 genes from obligate heterozygote individuals and CYP21A1P sequences from 59 control individuals indicated that p.P34L was not present in any gene or pseudogene sequences, whereas heterozygosis for p.H62L was observed in the pseudogene of four individuals (data not shown). Therefore, p.P34L seems to be a novel mutation not derived from pseudogene, whereas p.H62L showed a frequency of 3.4% in pseudogenes.

This study reports two novel deletion alleles in Brazilian patients with 21-hydroxylase deficiency and describes the variability of C4/CYP21 monomodular alleles evaluated by combining Southern blot, ASO-PCR, MLPA and sequencing techniques. The occurrence of different chimeric genes in Brazilian patients had not been reported before. Although Real-Time PCR and HLA-haplotypes would be alternative techniques to estimate, respectively, C4 and CYP21A2 copy number [35–37] and founder effect they were not available for this work.

By combining different techniques we characterized monomodular alleles carrying CYP21A1P/A2 chimeric genes in genotypes that were compound heterozygous with bi - or trimodular alleles bearing pseudogene-derived mutations, including a bimodular allele carrying p.R356W mutation associated to the rare 3.9-kb C4B fragment (table 2, patient 16; Figure 2c), described before in a non-disease causing allele [38]. Patient 9 who inherited from the mother the monomodular allele might also carry a tetramodular allele inherited from the father, however a more detailed study is required to confirm the tetramodular configuration for this allele that also carry a novel g.60G > A (TGG > TGA) nucleotide change causing the p.W19X mutation. The same mutation had been described before as a result of the TGG > TAG nucleotide change [39].

In general, data were convergent independently on the technique used. However, patients with alleles carrying a C4B/A or C4A/B gene and those in compound heterozygosis with trimodular alleles could be misinterpreted as carrying large gene conversions if only MLPA had been used, because C4 probes resulted in signals indicative of alleles without C4B deletion. Patients 1 and 2, are typical examples. The 6.4-kb Taq I fragment identified in patient 2 is generally a marker for a deletion that results from unequal crossover between a C4A ^[7.0] and a short C4B ^[5.4] gene [26, 40]. Such fragment is indicative of CYP21A1P deletion in monomodular alleles. It is found with a frequency of 11% in the general population and do not cause 21-hydroxylase deficiency [12] and would not be recognized in MLPA assay. The 6.4-kb gene variant is here described for the first time in association with a CYP21A1P/A2 gene in a case of 21-hydroxylase deficiency. Alleles bearing CYP21A1P deletions have been proposed as premutation for generating CYP21A2 deleted alleles [41]. It can be speculated that an allele bearing C4B/A ^[6.4] and CYP21A1P deletion might have influenced the formation of the monomodular allele in which the deleted allele seems to have been generated in at least two steps of unequal crossovers. However, those events must have happened several generations ago because the mutated allele had been segregating in this family for three generations. Additionally, those recombination events might have introduced novel nucleotide variants such as the -289T > C SNP in the 5'-promoter region of CYP21A1P/A2. The T variant at nucleotide 395, which is most frequent in CYP21A2 gene and a rare 1253G > A SNP within intron 5, which is described only in the CYP21A1P as a rare polymorphic nucleotide position, were also identified in this CYP21A1P/A2 chimeric gene. Therefore haplotype I was uniquely found in patient 2. In a paper published before [42], data obtained with ELISA assays also showed differences in C4 protein levels between patients 1 and 2. Low level of C4A protein was observed for patient 1 whereas patient 2 showed low level of C4B protein. Although C4A and C4B genes share 99% sequence identities, the proteins they encode have different hemolytic activities, covalent affinities to antigens and immune complexes, and serological reactivities [12, 43]. C4A gene copies producing proteins with electrophoretical characteristics of C4A but acting antigenically as C4B have been described in association to 30-kb deletion haplotypes [20, 44]. Differences conferring specific binding affinities are located within exon 26 [45], therefore monomodular allele in patient 1 may have 5'-end of C4A as indicated by 7.0-kb fragment and C4B sequences from exon 19 to 3'-end as indicated by MLPA and ELISA assays. Similarly, patients 5, 6 and 7 also carried a C4A ^[7.0] fragment with 3'-end C4B sequences as denoted by Southern blot and MLPA results. These patients together with patient 1 grouped within haplotype II, which is similar to those described in several populations [15, 20, 46, 47]. In addition, patient 20 showed positive signal for C4A gene but no signal for C4B probe (3:0) in MLPA. This result indicate that exon 17 in the C4B ^[6.0] gene probably corresponded to C4A sequences and the patient had been described as having very low immune response toward C4B antiserum [42]. Although this allele was not associated to 30-kb deletion, it illustrates C4 gene variability that influences MLPA results.

Both haplotypes III and IV carry a complete CYP21A1P pseudogene copy indicating that the recombination breakpoint should map within the 5 kb that separate 3'-end CYP21A2 and the exon 32 of TNXB gene. They differed because haplotype III showed the C allelic variants in both g.1645 and g.2110 (p.R356W) nucleotides whereas G and T, respectively, were observed in haplotype IV (table 3). Polymorphisms in CYP21A1P pseudogene are known to be common [40], therefore those haplotypes could be originated from unequal crossovers involving bimodular alleles carrying different pseudogene variants. Recombination within 3'-end CYP21A2 seems to be frequent since it has been reported by different research groups [15, 41] including as a de novo event in which deleted alleles were generated [48, 49].

A group of ten genes had recombination breakpoints identified between exon 3 and 4. Haplotype V diverged from the VI and VII because the alleles did not carry the pseudogene-derived p.P30L, but showed p.P34L and p.H62L mutations in exon 1. p.H62L has been recently described in association with p.P453S in patients with the NC form of 21-hydroxylase deficiency [50, 51]. In order to investigate whether p.P34L and p.H62L were rare pseudogene-derived mutations that have arisen in this chimeric gene through unequal crossover between gene and pseudogene, since they are flanked by CYP21A1P-like sequences, we tested 170 CYP21A2 genes from obligate heterozygous individuals and CYP21A1P sequences from 59 control individuals. Here we demonstrated that p.H62L might be originated in CYP21A1P since it was found in 3.4% pseudogene sequences. However, p.P34L was not found in any pseudogene sequences, therefore its origin remains unclear. Also, this haplotype showed the G variant at nucleotide -308 in the CYP21A1P/A2 5'-promoter region. Interestingly, this position is considered polymorphic only in CYP21A1P with frequencies varying from 0.1% to 0.3% in Chineses and Africans from Nigeria (NCBI-SNP database). Different mutations in exon 1 together with rare 5'-end SNP characterize a novel haplotype that seems to be frequent in Brazilian patients carrying monomodular alleles since it corresponded to 20% (4/20) of total 30-kb deleted alleles reported here as causing 21-hydroxylase deficiency. Probably, haplotype V have arisen in Brazil from an African ancestral since Brazilian population is highly miscigenated with populations from different origins including Africans of Benin Gulf region [52]. This haplotype might have segregated with 21-hydroxylase deficiency through an isolated founder effect for 30-kb deletion alleles. Main differences between haplotype VI and VII was found in -449 and g.395 nucleotides (table 3). The -449 position is considered to be ambiguous only in the pseudogene (SNP # rs28361032) whereas 395 is polymorphic in both gene and pseudogene sequences (SNP # rs6462) but there are no frequency data for the any of their allelic variants.

Haplotypes VIII and IX were separated because they showed different recombination breakpoints within intron 2. Those two haplotypes presented the CYP21A1P promoter region and p.P30L mutation as pseudogene-derived sequences and they are not very frequent in other populations [15, 53].

CYP21A1P/A2 chimeric genes can be correlated with SW or SV forms of 21-hydroxylase deficiency depending on the mutations they carry [15, 20, 46, 47]. The variability verified among 30-kb alleles with CYP21A1P/A2 chimeric genes present in different genotypes did not influence the phenotypes observed (tables 1, 2). Therefore, patients 1-6, 9-10 and 12-16 presented SW form of 21-hydroxylase deficiency as expected for homozygosis or compound heterozygosis for haplotypes I-VII and mutations that severely affect the enzyme activity (tables 1, 2). Similarly, compound heterozygote patients for haplotypes I-VII and p.I172N or p.V281L mutations presented, respectively, SV or NC forms of the disease (tables 1, 2, patients 7, 11, 17). Patients carrying haplotypes VIII and IX presented SV phenotype independently if they were compound heterozygous with a SV (tables 1, 2; p.I172N, patient 19) or SW mutations (tables 1, 2; p.Q318X and IVS2-13A/C > G, patients 18 and 20, respectively) indicating a synergistic effect of CYP21A1P promoter region and p.P30L upon the enzyme activity as proposed before [54].

Our study showed that the combination of Southern blot and ASO-PCR/direct sequencing with MLPA tests may constitute an option for mapping and better characterize chimeric genes on RCCX monomodular alleles, especially in populations with high allelic diversity such as that in Brazil. MLPA has been proposed as a candidate with good potential to be used in neo-natal screening and in pre-natal diagnosis because it can be performed with very low amount of DNA [55]. Eventually, MLPA may substitute time-consuming Southern blot in cases were HCA diagnosis is urgent as it managed to estimate the CYP21A1P/A2 borders in almost all cases. However, to distinguish between deletions and large gene conversions in genetic studies searching for detailed allelic information, it would be more informative if more C4 and CYP21 probes were included in the analysis.

Our study showed that the combination of Southern blot and ASO-PCR/direct sequencing with MLPA tests may constitute an option for mapping and better characterize chimeric genes on RCCX monomodular alleles, especially in populations with high allelic diversity such as that in Brazil. MLPA has been proposed as a candidate with good potential to be used in neo-natal screening and in pre-natal diagnosis because it can be performed with very low amount of DNA [55]. Eventually, MLPA may substitute time-consuming Southern blot in cases were HCA diagnosis is urgent as it managed to estimate the CYP21A1P/A2 borders in almost all cases. However, to distinguish between deletions and large gene conversions in genetic studies searching for detailed allelic information, it would be more informative if more C4 and CYP21 probes were included in the analysis.