A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern families

Arch Dermatol Res. 2009 Jun;301(5):391-3. doi: 10.1007/s00403-008-0903-9. Epub 2008 Sep 27.

Abstract

Autosomal recessive hypotrichosis simplex (ARHS) manifests with paucity of hair appearing during early childhood. We assessed four affected families. We initially genotyped three of these families for a panel of microsatellite markers spanning all ARHS-associated loci and obtained data suggesting linkage to 3q27, encompassing LIPH, which had previously been shown to be associated with ARHS. Accordingly, a homozygous duplication mutation in exon 2 of this gene (c.280_369dup; p.Gly94_Lys123dup) was found to segregate with the disease in all the families. Through the identification of the first duplication mutation in the human LIPH gene, we provide further evidence supporting a role for the phospholipase signalling pathway in hair growth and differentiation.

MeSH terms

  • Arabs*
  • Child
  • Chromosome Disorders / enzymology
  • Chromosome Disorders / genetics*
  • Chromosome Disorders / pathology
  • Chromosome Disorders / physiopathology
  • Chromosomes, Human, Pair 3
  • DNA Mutational Analysis
  • Exons / genetics
  • Gene Duplication*
  • Genes, Recessive
  • Genetic Predisposition to Disease
  • Hair / abnormalities
  • Hair / growth & development
  • Hair / pathology
  • Hair Follicle / growth & development
  • Hair Follicle / metabolism*
  • Hair Follicle / pathology
  • Humans
  • Hypotrichosis / enzymology
  • Hypotrichosis / genetics*
  • Hypotrichosis / pathology
  • Hypotrichosis / physiopathology
  • Israel
  • Lipase / genetics*
  • Lipase / metabolism
  • Microsatellite Repeats / genetics
  • Pedigree
  • Polymorphism, Genetic
  • Turkey

Substances

  • LIPC protein, human
  • Lipase