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Rapp-Hodgkin syndrome with pili canaliculi.
Pediatr Dermatol. 1993 Mar; 10(1):54-7.PD

Abstract

A 20-year-old woman and her 12-year-old brother had hypohidrotic ectodermal dysplasia, cleft lip and palate, midfacial hypoplasia with narrow nose from the nasal bridge to the tip, narrow dysplastic nails, and conical teeth and hypodontia, and hypospadias and hypoplastic uvula in the boy. The woman had major underdevelopment of intellectual capacity. The most important hair anomalies in both siblings were sparse eyebrows, pili torti, and pili canaliculi. Some of the pili canaliculi had two canals (pili bicanaliculi), and the cross section for scanning electron microscopy had a quadrangular aspect. This is the seventh family reported with Rapp-Hodgkin ectodermal dysplasia.

Authors+Show Affiliations

Department of Medico-Surgical Dermatology, Sevilla, Spain.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

8493170

Citation

Camacho, F, et al. "Rapp-Hodgkin Syndrome With Pili Canaliculi." Pediatric Dermatology, vol. 10, no. 1, 1993, pp. 54-7.
Camacho F, Ferrando J, Pichardo AR, et al. Rapp-Hodgkin syndrome with pili canaliculi. Pediatr Dermatol. 1993;10(1):54-7.
Camacho, F., Ferrando, J., Pichardo, A. R., Sotillo, I., & Jorquera, E. (1993). Rapp-Hodgkin syndrome with pili canaliculi. Pediatric Dermatology, 10(1), 54-7.
Camacho F, et al. Rapp-Hodgkin Syndrome With Pili Canaliculi. Pediatr Dermatol. 1993;10(1):54-7. PubMed PMID: 8493170.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Rapp-Hodgkin syndrome with pili canaliculi. AU - Camacho,F, AU - Ferrando,J, AU - Pichardo,A R, AU - Sotillo,I, AU - Jorquera,E, PY - 1993/3/1/pubmed PY - 1993/3/1/medline PY - 1993/3/1/entrez SP - 54 EP - 7 JF - Pediatric dermatology JO - Pediatr Dermatol VL - 10 IS - 1 N2 - A 20-year-old woman and her 12-year-old brother had hypohidrotic ectodermal dysplasia, cleft lip and palate, midfacial hypoplasia with narrow nose from the nasal bridge to the tip, narrow dysplastic nails, and conical teeth and hypodontia, and hypospadias and hypoplastic uvula in the boy. The woman had major underdevelopment of intellectual capacity. The most important hair anomalies in both siblings were sparse eyebrows, pili torti, and pili canaliculi. Some of the pili canaliculi had two canals (pili bicanaliculi), and the cross section for scanning electron microscopy had a quadrangular aspect. This is the seventh family reported with Rapp-Hodgkin ectodermal dysplasia. SN - 0736-8046 UR - https://www.unboundmedicine.com/medline/citation/8493170/Rapp_Hodgkin_syndrome_with_pili_canaliculi_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0736-8046&date=1993&volume=10&issue=1&spage=54 DB - PRIME DP - Unbound Medicine ER -