Journal
CLINICAL AND EXPERIMENTAL DERMATOLOGY
Volume 40, Issue 1, Pages 78-84Publisher
WILEY-BLACKWELL
DOI: 10.1111/ced.12457
Keywords
-
Categories
Funding
- Pakistan Academy of Sciences (PAS), Islamabad, Pakistan
Ask authors/readers for more resources
BackgroundAutosomal recessive hypotrichosis is a rare human hereditary disorder presenting as sparse scalp hair or as woolly hair occurring on various parts of the body. Various forms of isolated hypotrichosis have been reported to date. Mutations in at least 11 genes have been reported to cause hypotrichosis. AimsTo investigate the clinical and genetic basis of autosomal recessive hypotrichosis in two unrelated consanguineous families. MethodsGenotyping by highly polymorphic microsatellite markers established linkage in both families to the DSG4 gene on chromosome 18q21. PCR amplification of exons and intron-exon borders of the DSG4 gene was performed, and the products sequenced to search for disease-causing sequence variants. ResultsClinical investigation revealed typical hypotrichosis in the affected members of one family, while other affected members showed presence of monilethrix-like scalp hair. Sequence analysis of DSG4 revealed a novel deletion mutation (c.85-1_191del) in the affected subjects of both families. ConclusionsThis study further extends the body of evidence that mutations in the DSG4 gene result in both hypotrichosis and monilethrix-like scalp hair.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available