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Hereditary hypotrichosis simplex of the scalp.
Dermatology. 1995; 191(2):139-41.D

Abstract

We report on a female aged 13 years, whose scalp hair began to disappear at the age of 9 years, leaving only sparse wispy hairs in the parietal-occipital region. Eyelashes, eyebrows and body hair were unaffected. There were no signs of ectodermal dysplasia on the skin, nails, teeth and eyes nor other congenital abnormalities. The family pedigree showed 15 relatives similarly affected according to an autosomal dominant mode of transmission. Clinical, genetic, histological and ultrastructural aspects led to a diagnosis of hereditary hypotrichosis simplex of the scalp (Toribio-Quiñones type).

Authors+Show Affiliations

Department of Dermatology, University Hospital, Universidad de Salamanca, Spain.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

8520061

Citation

Rodríguez Díaz, E, et al. "Hereditary Hypotrichosis Simplex of the Scalp." Dermatology (Basel, Switzerland), vol. 191, no. 2, 1995, pp. 139-41.
Rodríguez Díaz E, Fernández Blasco G, Martín Pascual A, et al. Hereditary hypotrichosis simplex of the scalp. Dermatology. 1995;191(2):139-41.
Rodríguez Díaz, E., Fernández Blasco, G., Martín Pascual, A., & Armijo, M. (1995). Hereditary hypotrichosis simplex of the scalp. Dermatology (Basel, Switzerland), 191(2), 139-41.
Rodríguez Díaz E, et al. Hereditary Hypotrichosis Simplex of the Scalp. Dermatology. 1995;191(2):139-41. PubMed PMID: 8520061.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Hereditary hypotrichosis simplex of the scalp. AU - Rodríguez Díaz,E, AU - Fernández Blasco,G, AU - Martín Pascual,A, AU - Armijo,M, PY - 1995/1/1/pubmed PY - 1995/1/1/medline PY - 1995/1/1/entrez SP - 139 EP - 41 JF - Dermatology (Basel, Switzerland) JO - Dermatology VL - 191 IS - 2 N2 - We report on a female aged 13 years, whose scalp hair began to disappear at the age of 9 years, leaving only sparse wispy hairs in the parietal-occipital region. Eyelashes, eyebrows and body hair were unaffected. There were no signs of ectodermal dysplasia on the skin, nails, teeth and eyes nor other congenital abnormalities. The family pedigree showed 15 relatives similarly affected according to an autosomal dominant mode of transmission. Clinical, genetic, histological and ultrastructural aspects led to a diagnosis of hereditary hypotrichosis simplex of the scalp (Toribio-Quiñones type). SN - 1018-8665 UR - https://wwww.unboundmedicine.com/medline/citation/8520061/Hereditary_hypotrichosis_simplex_of_the_scalp_ L2 - https://www.karger.com?DOI=10.1159/000246532 DB - PRIME DP - Unbound Medicine ER -