Document Detail

Familial erythromelanosis follicularis faciei et colli--an autosomal recessive mode of inheritance.
MedLine Citation:
PMID:  8348729     Owner:  NLM     Status:  MEDLINE    
Two cases of erythromelanosis follicularis faciei et colli in one family, affecting a brother and sister are described. In these cases erythromelanosis follicularis faciei et colli, a process of unknown aetiology, seems to have a clear hereditary component--autosomal recessive mode of inheritance--a feature which, as far as we know, has not been reported in the literature.
S Yañez; J A Velasco; M P González
Related Documents :
2848459 - Adenovirus infection in families.
17228159 - Short femurs detected at 25 and 31 weeks of gestation diagnosed as leroy i-cell disease...
16188369 - Natural history of familial myomas.
20955989 - Familial cystic teratomas: four case reports and review of the literature.
16884599 - Pigmented mesenteric lymphadenopathy in familial adenomatous polyposis - an unusual cau...
3598129 - Pelizaeus-merzbacher disease: clinical and nosological study.
6932149 - Cells of nucleus pulposus in cerebrospinal fluid: a case report.
22937369 - Ewing's sarcoma of the zygomatic arch presenting in a 69-year old: an unusual case report.
20422419 - Cutaneous endometriosis: review of 15 cases diagnosed at a single institution.
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Clinical and experimental dermatology     Volume:  18     ISSN:  0307-6938     ISO Abbreviation:  Clin. Exp. Dermatol.     Publication Date:  1993 May 
Date Detail:
Created Date:  1993-09-13     Completed Date:  1993-09-13     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  7606847     Medline TA:  Clin Exp Dermatol     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  283-5     Citation Subset:  IM    
Department of Dermatology, Clinical Hospital, University of Salamanca, Spain.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Erythema / genetics*
Facial Dermatoses / genetics*
Melanosis / genetics*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Benign cephalic histiocytosis--study of a case.
Next Document:  Secondary localized cutaneous amyloid in Bowen's disease.