Literature DB >> 11298530

Homozygosity at chromosome 8qter in individuals affected by mal de Meleda (Meleda disease) originating from the island of Meleda.

H Patel1, M Nardelli, T Fenn, R Houlston, A Coonar, M A Patton, A H Crosby.   

Abstract

BACKGROUND: The inherited palmoplantar keratodermas (PPKs) are a clinically heterogeneous group of disorders characterized by thickening of the skin of the palms and the soles. These diseases also exhibit genetic heterogeneity and many autosomal dominant and recessive forms have been described. Mal de Meleda (Meleda disease, MD) is an autosomal recessive form of PPK first described on the Dalmatian island of Meleda. A gene for MD has recently been assigned to the most telomeric portion of chromosome 8q using two large Algerian families.
OBJECTIVES: To determine whether the same gene underlies the skin disease in Meleda islanders.
METHODS: We have examined five affected individuals originating from the Dalmatian island itself for 8qter homozygosity.
RESULTS: This region was found to be homozygous in all five affected individuals but in none of the 20 other unaffected family members examined.
CONCLUSIONS: The current study confirms the localization of a gene for MD to 8qter using samples from the island of Meleda, highlighting the clinical and genetic homogeneity of this condition.

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Year:  2001        PMID: 11298530     DOI: 10.1046/j.1365-2133.2001.04127.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  2 in total

Review 1.  Mendelian diseases and conditions in Croatian island populations: historic records and new insights.

Authors:  Vanja Saftić; Diana Rudan; Lina Zgaga
Journal:  Croat Med J       Date:  2006-08       Impact factor: 1.351

2.  Further evidence of the clinical and genetic heterogeneity of recessive transgressive PPK in the Mediterranean region.

Authors:  Cherine Charfeddine; Mourad Mokni; Selma Kassar; Hela Zribi; Chiraz Bouchlaka; Samir Boubaker; Ahmed Rebai; Amel Ben Osman; Sonia Abdelhak
Journal:  J Hum Genet       Date:  2006-07-25       Impact factor: 3.172

  2 in total

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