Original Article

Subject Category: Genetics

Journal of Investigative Dermatology (2009) 129, 1927–1934; doi:10.1038/jid.2009.19; published online 5 March 2009

Founder Mutations in the Lipase H Gene in Families with Autosomal Recessive Woolly Hair/Hypotrichosis

Yutaka Shimomura1, Muhammad Wajid1, Abraham Zlotogorski2, Young-Jin Lee3, Robert H Rice4 and Angela M Christiano1,5

  1. 1Department of Dermatology, Columbia University, New York, New York, USA
  2. 2Department of Dermatology and the Center for Genetic Diseases of the Skin and Hair, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
  3. 3Proteomics Core Facility, Genome Center, University of California, Davis, California, USA
  4. 4Department of Environmental Toxicology, University of California, Davis, California, USA
  5. 5Department of Genetics and Development, Columbia University, New York, New York, USA

Correspondence: Dr Angela M. Christiano, Department of Dermatology, College of Physicians and Surgeons, Columbia University, 630 West 168th Street VC-15, New York, New York 10032, USA. E-mail: amc65@columbia.edu

Received 17 September 2008; Revised 4 December 2008; Accepted 27 December 2008; Published online 5 March 2009.

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Abstract

Autosomal-recessive woolly hair (ARWH)/hypotrichosis is a hereditary hair disorder which is characterized by tightly curled hair and is associated with sparse hair. ARWH can be caused by mutations in the P2RY5 or lipase H (LIPH) gene. Disruption of either gene results in phenotypes with features of both wooly hair (WH) and hypotrichosis. In this study, we identified two Guyanese families with ARWH. Both families are of recent Indian descent. Mutation analysis resulted in the identification of mutations in the LIPH gene in both families. Affected individuals in the first family carry compound heterozygous mutations Ex7_8del and 1303_1309dupGAAAACG in the LIPH gene, while those in the second family have a homozygous mutation 659_660delTA in the LIPH gene. The mutations Ex7_8del and 659_660delTA were identified earlier in several Pakistani families with ARWH. Haplotype analysis using microsatellite markers close to the LIPH gene defined a founder haplotype shared in families from Pakistan and Guyana. Proteomic analysis of hair shaft samples from one of the families revealed no substantial changes among the proteins identified, indicating that the syndrome does not involve global alterations in protein expression. Our results further suggest a crucial role of LIPH gene in hair growth.

Abbreviations:

ARWH, autosomal-recessive woolly hair; HF, hair follicle; LIPH gene, lipase H; WH, wooly hair

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