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Fig. 2 | BMC Medical Genetics

Fig. 2

From: A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani family

Fig. 2

Phenotypes of affected members. Complete absence of hairs on scalp, eyebrows, eyelashes and rest of the body of individual IV-1 (a). Note dystrophic, irregularly shaped nails at the distal portion and distal onycholysis of the digits on hands and toe nails dystrophy in affected members IV-1 (b, c), IV-3 (d, e) and IV-4 (f, g)

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BMC Medical Genetics

ISSN: 1471-2350

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