- Research article
- Open Access
- Open Peer Review
An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3
© Bouhouche et al; licensee BioMed Central Ltd. 2012
- Received: 19 September 2011
- Accepted: 21 March 2012
- Published: 21 March 2012
Single-gene disorders related to ischemic stroke seem to be an important cause of stroke in young patients without known risk factors. To identify new genes responsible of such diseases, we studied a consanguineous Moroccan family with three affected individuals displaying hereditary leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa that appears to segregate in autosomal recessive pattern.
All family members underwent neurological and radiological examinations. A genome wide search was conducted in this family using the ABI PRISM linkage mapping set version 2.5 from Applied Biosystems. Six candidate genes within the region linked to the disease were screened for mutations by direct sequencing.
Evidence of linkage was obtained on chromosome 17q24.2-25.3. Analysis of recombination events and LOD score calculation suggests linkage of the responsible gene in a genetic interval of 11 Mb located between D17S789 and D17S1806 with a maximal multipoint LOD score of 2.90. Sequencing of seven candidate genes in this locus, ATP5H, FDXR, SLC25A19, MCT8, CYGB, KCNJ16 and GRIN2C, identified three missense mutations in the FDXR gene which were also found in a homozygous state in three healthy controls, suggesting that these variants are not disease-causing mutations in the family.
A novel locus for leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa has been mapped to chromosome 17q24.2-25.3 in a consanguineous Moroccan family.
- Ischemic Stroke
- Fabry Disease
- Retinitis Pigmentosa
- Moyamoya Disease
- Genome Wide Search
Nuclear single-gene disorders related to ischemic stroke are an important cause of stroke, especially in young patients without known risk factors . These diseases could be associated with different stroke phenotypes including arterial dissection, small vessel, and large vessel which are inherited as dominant, recessive or X linked trait. Up to date, 4 loci have been described for the autosomal dominant form. Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) which is a generalized disease of the small arteries, largely predominating in the brain caused by mutations in NOTCH3 gene [2, 3]. Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS) is a rare multisystemic disease presenting with leukoencephalopathy, progressive visual loss and nephropathy due to mutations in the TREX1 gene . Marfan syndrome (MFS) which is a connective tissue disorder with multisystemic manifestations involving skeletal, cardiovascular and ocular systems caused by mutations in a very large gene FBN1 . The Ehlers-Danlos syndrome type IV (EDS) is a connective tissue disorder defined by characteristic facial features, translucent skin, easy bruising, and severe arterial, digestive and uterine complications resulting from mutations in COL3A1 gene .
In addition to the autosomal dominant forms, three autosomal recessive forms have been also reported. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) is a cerebral small vessel disease accompanied by alopecia and spondylosis caused by mutations in the HTRA1 gene . Pseudoxanthoma elasticum (PXE), associated with stenotic lesions of the distal carotid artery and with small vessel disease, is characterized by skin, eyes, and cardiovascular complications and related to mutations in the ABCC6 gene on chromosome 16p13.1 . The homocystinuria is characterized by developmental delay/intellectual disability, ectopia lentis and/or severe myopia, skeletal abnormalities and thromboembolism caused by mutations in the CBS gene .
Fabry disease (FD) is a progressive X-linked inherited disorder of glycosphingolipid metabolism due to deficient or absent lysosomal alpha-galactosidase A activity. FD is associated with Cerebrovascular symptoms due to the damage of small and large blood vessels, progressive renal failure, cardiac disease, small-fiber peripheral neuropathy, and skin lesions caused by mutation in the GLA gene at Xq22 .
Finally, Moyamoya disease (MMD), characterized by bilateral stenosis and/or occlusion of the terminal portion of the internal carotid artery, could be inherited as dominant, recessive and X-linked trait [11, 12]. Several genetic loci have been reported on chromosomes 3p, 6q and 17q but none of the relevant genes have yet been identified [13–16].
In the present study, we report on a consanguineous Moroccan family with three patients displaying an autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa. The genome wide search mapped this new clinical entity to a new locus on chromosome 17q24.2-25.3 in a chromosomal segment of 11 Mb.
Genotyping and linkage analysis
A genome-wide search was conducted using the ABI PRISM linkage mapping set version 2.5 from Applied Biosystems. The set consists of 400 fluorescent microsatellite markers, selected from the Généthon human linkage map covering the entire human genome with a resolution of approximately 10 cM. These markers were PCR amplified according to the manufacturer's instructions. PCR products of each panel were then pooled, combined in a tube with GeneScan 500LIZ size standard and loaded in an automated capillary DNA sequencer ABI 310. Data were collected and analysed using the ABI GENESCAN (version 2.1) and GENOTYPER (version 2.0) software (Applied Biosystems, Foster City, CA). The C.E.P.H. 1347-02 DNA was used as control.
On the basis of the segregation pattern observed in the studied family, pairwise and multipoint LOD scores were calculated using the Allegro v1.2c2 software , assuming a fully penetrant autosomal recessive trait with a disease allele frequency of 0.00005, 0% phenocopy and equal recombination fraction in males and females. Haplotypes were constructed according to the principles of Thomson (1987). The order and distance between markers were that of the ensembl.org genetic map.
Sequencing of candidate genes
The 5' and 3' UTRs and all the coding exons, including exon-intron boundaries, of seven candidate genes were amplified by PCR and both strands were sequenced using Big Dye Terminator Cycle Ready Reaction Kits (Applied Biosystems) on an ABI 310 sequencer. Sequence chromatograms were analyzed using SeqScape software version 2.1 (Applied Biosystems).
In the family we investigated here, the healthy parents and grand-parents of the affected siblings were first cousins and representing one of the four consanguinity loops in the pedigree. Thus, the segregation of the disease was in favor of an autosomal recessive mode of inheritance.
Patient V.2, a 33-year-old female, was a full-term baby girl with no history of a neonatal suffering or infection as well. Since the age of 5, she presented late psychomotor acquisitions and abnormal crawling movements of both arms. She didn't have any seizure or motor loss. Neurological exam at age 33 years showed mental retardation, neck dystonia, and dysmorphic syndrome with an oblong face, hypertelorism, arched palate, macroglossia and pes cavus. Cardiac exam found a heart murmur of mitral regurgitation and a hepatojugular reflux with hepatomegaly. Ophthalmologic exam found myopic chorioretinal degenerative lesions, with papillary pallor and fine vessels, and retinitis pigmentosa. Axial T2-weighted and FLAIR images showed multiple Focal white-matter hyperintensities (Figure 2C) and MR spectroscopy performed at different levels showed a small peak of lactate (Figure 2D). ENMG was difficult to perform but showed no signs of neuropathy. EEG found a normal background activity with no epileptic abnormalities. ECG showed a left ventricular hypertrophy with regular sinusal rhythm and normal echocardiography. Morphological analysis of muscle-biopsy showed no signs of atrophy or dystrophy. The histochemical analysis (NADH, SDH and COX) were normal and no red ragged fibers were seen. Blood analysis showed normal level of lactate at 181 mg/l. Cortisol (4.8 μg/dl). Electrolytes, urea, creatinin, hepatic enzymes were also normal. Amino acid chromatography showed elevated blood levels of glutamine, glycine, alanine and glutamate and elevated levels of urinary glycine and basic amino acids.
Patient V.4, a 27-year-old male, presented at the age of 7 months a fever and dystonic movements. He had late psychomotor development, as he walked at age of 7 years and did not talk; he also had an autistic behaviour. At the age of 17, he had several generalised seizures. Neurological exam at age 27 years found mental retardation, generalised dystonia, and pyramidal syndrome, along with a dysmorphic syndrome including hypertelorism, arched palate and dorsal scoliosis. Brain CT scan showed a left systemised temporoparietal hypodensity and another right temporo-occipital hypodensity evoking sequellar vascular lesions (data not shown). Axial T2-weighted and FLAIR images at different levels showed a sequellar ischemic stroke of the left posterior sylvian territory (Figure 2B). The MRA was normal and did not show signs of Moyamoya disease. Blood investigations found low level of cholesterol 1.41 g/l (normal 1.50-2.50) and normal level of cortisol (6.2 μg/dl). Metanephrin (0.08 mg/24 h), normetanephrin (0.17 mg/24 h), corticotrophin (17.9 ng/l), ApoA1 (0.84 g/l) and ApoB (0.53 g/l) were also normal. He presented several episodes of severe hypochromic microcytic anemia which required blood transfusion. Amino acid chromatography showed an elevation of blood levels of glutamine, glycine, alanine and glutamate and elevated levels of urinary glycine and basic amino acids. Chromosomal analysis showed a normal karyotype in the 11 observed metaphase cells.
Mapping and sequencing of candidate genes
Two point LOD score for microsatellite markers of family RBT-DAK calculated at recombination fraction θ = 0
θ = 0.00
This new genetic locus contains ≈ 140 known genes according to the genome database (Ensembl.org). The large clinical spectrum of the disease in the family RBT-ENC and the presence of small peak of lactate found in MR spectroscopy, make the three genes that encode proteins with known mitochondrial functions strong candidate for the disease. These include ATP5H, FDXR and SLC25A19 encoding ATP synthase subunit d, ferredoxin-NADP (+) reductase and solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 respectively. Since mutations in MCT8 gene lead to a syndrome of severe psychomotor retardation , we also sequenced MCT6 encoding the monocarboxylic acid transporter 7. We next analyzed the CYGB gene, encoding a cytoglobin which may be involved in oxygen storage and delivery and may acts as an endogenous neuroprotective factor in focal cerebral ischemia . Since glutamate and N-methyl-D-aspartate (NMDA) receptors have been implicated in several disorders of the central nervous system including stroke  and GRIN2A and GRIN2B genes have been recently implicated in encephalopathy with mental retardation and epilepsia , we sequenced the GRIN2C gene encoding the glutamate receptor, ionotropic, N-methyl D-aspartate 2 C. We also sequenced the KCNJ16 gene since KCNJ2 and KCNJ10 have been associated with mental retardation, dysmorphic syndrome and a CNS phenotype [22, 23]. No causative mutations were identified in the coding sequence of all these genes. However, in the FDXR gene, we found three missense mutations reported as SNP in ensembl.org data base (rs1688149 (c.275A > G/p.Asp92Gly); rs690514 which was found in 4 transcripts (c.368 G > A/Arg123Gln; c.461 G > A/p.Arg154Gln; c.497 G > A/p.Arg166Gln; c.236 G > A/p.Arg79Gln); and rs552432 (c.887 T > C/p.Leu296Pro)) at homozygous state in all patients and segregated with the disease in the family. Sequencing of 60 DNA individual controls showed that 20/60 presented this haplotype with the three mutations at heterozygous state and 3/60 at homozygous state. As the disease is considered very rare, these variants should be polymorphism rather than causal mutations.
Consanguineous families with rare disease are extremely useful in defining new loci for autosomal recessive diseases. In the family investigated here, the segregation of the disease was in favor of an autosomal recessive mode of inheritance. In all patients, the disease starts in early infancy by psychomotor retardation and progressive dystonic and choreic movements. At age of exam, all patients presented severe mental impairment, dysmorphic syndrome and retinitis pigmentosa. Only patient V.4 had epilepsia with several episodes of generalized seizures. Radiological investigations showed multiple ischemic lesions interesting small arteries in two patients (V.1 and V.2) and large artery in patient V.4, whereas MRA was normal in this patient. The clinical presentation was therefore associated in the studied family with leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa. Suggestive linkage of the responsible gene was found on chromosome 17q24.2-25.3 in an 11 Mb genetic interval between D17S789 and D17S1806 with a maximal multipoint LOD score of 2.90. Two loci of Autosomal dominant Moyamoya disease have been mapped to chromosome 17q. The locus of Mineharu et al. (2008) was distal to D17S1806 marker and thus did not overlap with our new locus. However, it overlaps with the locus of Yamauchi T et al. (2000) but the clinical presentation in the family studied here was different of the one reported for Moyamoya disease.
Seven candidate genes in this locus, ATP5H, FDXR, SLC25A19, MCT8, CYGB, KCNJ16 and GRIN2C were sequenced but no causative mutation was found. The clinical presentation is very broad in the family studied here and suggests that the disease could be due to a nuclear mitochondrial gene, but the lactate level was normal in blood and MR spectroscopy showed only small peak of lactate. However, the elevated levels of amino acids observed in the blood and urine rather suggest that the defective gene may be involved in pathways of intermediary metabolism. In these pathways, amino acids, when deaminated, yield α-keto acids that, directly or via additional reactions, feed into the major metabolic pathways (e.g., Krebs cycle). More families with the same disease showing linkage to this locus are needed to reduce the candidate genetic interval and thus the number of genes to be analyzed.
We report here the identification of a novel locus for autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa on chromosome 17q24.2-25.3, in a genetic interval of 11 Mb. Gene identification is ongoing and should increase our understanding of the causes and the physiopathology of this ischemic stroke condition.
We thank all family members for their cooperation throughout this study. Written consent for publication was obtained from the father of patients. We thank Prof. Rachid TAZI-AHNINI from Sheffield University for revising the manuscript. This work was supported by the Centre National de Recherche Scientifique et Technique (CNRST) of Ministry of High Education and Research, Morocco; and the University Mohamed V - Souissi (Rabat, Morocco). A Bouhouche, A.B., L.E., L.L., N.B., J.A., S.S., E.C., E.E. and M.Y. are members of the Moroccan 'Pôle de Compétences en Neurogénétique' research network.
- Meschia JF: New information on the genetics of stroke. Curr Neurol Neurosci Rep. 2011, 11: 35-41. 10.1007/s11910-010-0155-x.View ArticlePubMedPubMed CentralGoogle Scholar
- Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cécillion M, Marechal E, Maciazek J, Vayssiere C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E: Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature. 1996, 383: 707-710. 10.1038/383707a0.View ArticlePubMedGoogle Scholar
- Tang SC, Jeng JS, Lee MJ, Yip PK: Notch signaling and CADASIL. Acta Neurol Taiwan. 2009, 18: 81-90.PubMedGoogle Scholar
- Richards A, van den Maagdenberg AM, Jen JC, Kavanagh D, Bertram P, Spitzer D, Liszewski MK, Barilla-Labarca ML, Terwindt GM, Kasai Y, McLellan M, Grand MG, Vanmolkot KR, de Vries B, Wan J, Kane MJ, Mamsa H, Schäfer R, Stam AH, Haan J, de Jong PT, Storimans CW, van Schooneveld MJ, Oosterhuis JA, Gschwendter A, Dichgans M, Kotschet KE, Hodgkinson S, Hardy TA, Delatycki MB, Hajj-Ali RA, Kothari PH, Nelson SF, Frants RR, Baloh RW, Ferrari MD, Atkinson JP: C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy. Nat Genet. 2007, 39: 1068-1070. 10.1038/ng2082.View ArticlePubMedGoogle Scholar
- Leibrero A, Martins E, Cruz C, Almeida J, Maciel MJ, Cardoso JC, Lima CA: Marfan syndrome: clinical manifestations, pathophysiology and new outlook on drug therapy. Rev Port Cardiol. 2010, 29: 1021-1036.Google Scholar
- Watanabe A, Shimada T: Vascular type of Ehlers-Danlos syndrome. J Nippon Med Sch. 2008, 75: 254-261. 10.1272/jnms.75.254.View ArticlePubMedGoogle Scholar
- Hara K, Shiga A, Fukutake T, Nozaki H, Miyashita A, Yokoseki A, Kawata H, Koyama A, Arima K, Takahashi T, Ikeda M, Shiota H, Tamura M, Shimoe Y, Hirayama M, Arisato T, Yanagawa S, Tanaka A, Nakano I, Ikeda S, Yoshida Y, Yamamoto T, Ikeuchi T, Kuwano R, Nishizawa M, Tsuji S, Onodera O: Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease. N Engl J Med. 2009, 360: 1729-1739. 10.1056/NEJMoa0801560.View ArticlePubMedGoogle Scholar
- Finger RP, Charbel Issa P, Ladewig MS, Götting C, Szliska C, Scholl HP, Holz FG: Pseudoxanthoma elasticum: genetics, clinical manifestations and therapeutic approaches. Surv Ophthalmol. 2009, 54: 272-285. 10.1016/j.survophthal.2008.12.006.View ArticlePubMedGoogle Scholar
- Dichgans M: Genetics of ischaemic stroke. Lancet Neurol. 2007, 6: 149-161. 10.1016/S1474-4422(07)70028-5.View ArticlePubMedGoogle Scholar
- Schiffmann R: Fabry disease. Pharmacol Ther. 2009, 122: 65-77. 10.1016/j.pharmthera.2009.01.003.View ArticlePubMedGoogle Scholar
- Takahachi JC, Miyamoto S: Moyamoya disease: recent progress and outlook. Neurol Med Chir (Tokyo). 2010, 50: 824-832. 10.2176/nmc.50.824.View ArticleGoogle Scholar
- Herve D, Touraine P, Verloes A, Miskinyte S, Krivosic V, Logeart D, Alili N, Laredo JD, Gaudric A, Houdart E, Metzger JP, Tournier-Lasserve E, Woimant F: A hereditary moyamoya syndrome with multisystemic manifestations. Neurology. 2010, 75: 259-264. 10.1212/WNL.0b013e3181e8ee3f.View ArticlePubMedGoogle Scholar
- Ikeda H, Sasaki T, Yoshimoto T, Arinami T: Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26. Am J Hum Genet. 1999, 64: 533-537. 10.1086/302243.View ArticlePubMedPubMed CentralGoogle Scholar
- Inoue TK, Ikezaki K, Sasazuki T, Matsushima T, Fukui M: Linkage analysis of moyamoya disease on chromosome 6. J Child Neurol. 2000, 15: 179-182. 10.1177/088307380001500307.View ArticlePubMedGoogle Scholar
- Yamauchi T, Tada M, Houkin K, Tanaka T, Nakamura Y, Kuroda S, Abe H, Inoue T, Ikezaki K, Matsushima T, Fukui M: Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25. Stroke. 2000, 31: 930-935. 10.1161/01.STR.31.4.930.View ArticlePubMedGoogle Scholar
- Mineharu Y, Liu W, Inoue K, Matsuura N, Inoue S, Takenaka K, Ikeda H, Houkin K, Takagi Y, Kikuta K, Nozaki K, Hashimoto N, Koizumi A: Autosomal dominant moyamoya disease maps to chromosome 17q25.3. Neurology. 2008, 70: 2357-2363. 10.1212/01.wnl.0000291012.49986.f9.View ArticlePubMedGoogle Scholar
- Gudbjartsson DF, Jonasson K, Frigge ML, Kong A: Allegro, a new computer program for multipoint linkage analysis. Nat Genet. 2000, 25: 12-13. 10.1038/75514.View ArticlePubMedGoogle Scholar
- van der Deure WM, Peeters RP, Visser TJ: Molecular aspects of thyroid hormone transporters, including MCT8, MCT10, and OATPs, and the effects of genetic variation in these transporters. J Mol Endocrinol. 2010, 44: 1-11. 10.1677/JME-09-0042.View ArticlePubMedGoogle Scholar
- Fordel E, Geuens E, Dewilde S, De Coen W, Moens L: Hypoxia/ischemia and the regulation of neuroglobin and cytoglobin expression. IUBMB Life. 2004, 56: 681-687. 10.1080/15216540500037406.View ArticlePubMedGoogle Scholar
- Gogas KR: Glutamate-based therapeutic approaches: NR2B receptor antagonists. Curr Opin Pharmacol. 2006, 6: 68-74. 10.1016/j.coph.2005.11.001.View ArticlePubMedGoogle Scholar
- Endele S, Rosenberger G, Geider K, Popp B, Tamer C, Stefanova I, Milh M, Kortüm F, Fritsch A, Pientka FK, Hellenbroich Y, Kalscheuer VM, Kohlhase J, Moog U, Rappold G, Rauch A, Ropers HH, von Spiczak S, Tönnies H, Villeneuve N, Villard L, Zabel B, Zenker M, Laube B, Reis A, Wieczorek D, Van Maldergem L, Kutsche K: Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. Nat Genet. 2010, 42: 1021-1026. 10.1038/ng.677.View ArticlePubMedGoogle Scholar
- Rajakulendran S, Tan SV, Hanna MG: Muscle weakness, palpitations and a small chin: the Andersen-Tawil syndrome. Pract Neurol. 2010, 10: 227-231. 10.1136/jnnp.2010.217794.View ArticlePubMedGoogle Scholar
- Scholl UI, Choi M, Liu T, Häusler MG, Grimmer J, Tobe SW, Farhi A, Nelson-Williams C, Lifton RP: Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10. Proc Nat Acad Sci USA. 2009, 106: 5842-5847. 10.1073/pnas.0901749106.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2350/13/18/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.