Clinical and genetic studies of 3 large, consanguineous, Algerian families with Mal de Meleda

Archives of Dermatology

Volumn 136, Issue 10, 2000, Pages 1247-1252

  Bouadjar, Bakar ^a   Benmazouzia, Smaïl ^a   Prud'homme, Jean François ^b   Cure, Susan ^c   Fischer, Judith ^b  

^a Bab El Oued Hospital   (Algeria)

^b GÉNÉTHON   (France)

^c CENTRE NATIONAL DE SÉQUENÇAGE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

SALICYLIC ACID;

ADOLESCENT; ADULT; ALGERIA; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BRACHYDACTYLY; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE ASSOCIATION; ERYTHEMA; ETHNOLOGY; FAMILIAL DISEASE; FEMALE; GENE MAPPING; GENETIC ANALYSIS; GENETIC LINKAGE; GENODERMATOSIS; HISTOPATHOLOGY; HOMOZYGOSITY; HUMAN; HYPERHIDROSIS; KERATOSIS PALMOPLANTARIS; KERATOSIS PALMOPLANTARIS TRANSGREDIENS OF SIEMENS; LICHENOID; MAL DE MELEDA; MALE; NAIL DISEASE; PEDIGREE; PREVALENCE; PRIORITY JOURNAL;

EID: 0033769957     PISSN: 0003987X     EISSN: None     Source Type: Journal    
DOI: 10.1001/archderm.136.10.1247     Document Type: Article

References (32)

1. Mal de Meleda
2. Ueber keratoma hereditarum
3. Vererbungverhaltnisse bei der sog Krankheit von Mljet (mal de Meleda)
4. La maladie de Meleda autochtone
5. Genetic linkage of Meleda disease to chromosome 8qter
6. Mal de Meleda in a Laotian family
7. La keratodermie palmo-plantaire type Meleda
8. Mal de Meleda: A report of four cases from the United Arab Emirates
9. Homozygosity mapping: A way to map human recessive traits with the DNA of inbred children
10. Mapping of Papillon-Lefevre syndrome to the chromosome 11q14 region
11. Multilocus linkage analysis in humans: Detection and estimation of recombination
12. Differential diagnosis of plantar palmar keratoderma
13. Deux cas de keratodermie palmaire et plantaire symetrique familiale (maladie de Meleda) chez le frere et la soeur: Coexistence darts les deux cas d'alterations dentaires graves
14. Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis
15. Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK)
16. A mutation in the V1 end domain of keratin 1 in non-epidermolytic palmar-plantar keratoderma
17. Keratoderma hereditaria mutilans (Vohwinkel): Differentiating features of conditions with constriction of digits
18. A missense mutation in connexin 26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families
19. A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome
20. The molecular pathology of progressive symmetric erythrokeratoderma: A frame-shift mutation in the loricrin gene and perturbations in the cornified cell envelope
21. Mutations in human connexin gene GJB3 cause erythrokeratodermia variabilis
22. Hereditary palmoplantar keratosis of the Gamborg Nielsen type: Clinical and ultrastructural characteristics of a new type of autosomal recessive palmoplantar keratosis
23. Mal de Meleda: Review of the literature and report of four cases
24. Ceratoma palmate et plantare transgrediens mal de Meleda
25. Die krankheit von Meleda
26. Type sclerodermiforme de la maladie de Meleda
27. Unusual cases of Meleda keratoderma treated with aromatic retinoid etretinate
28. Palmar and plantar hyperkeratosis of the Meleda type
29. Report of a family with mal de Meleda in Taiwan: A clinical, histopathological and immunological study
30. Mal de Meleda
31. Mal de Meleda treated with 13-cis retinoic acid
32. Bie Meleda-krankheiteine akroerythrokeratodermie