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GAPO syndrome: a report of two siblings and a review of literature.
Pediatr Dermatol. 2010 Mar-Apr; 27(2):156-61.PD

Abstract

Growth retardation, alopecia, pseudoanodontia, optic atrophy (GAPO) syndrome is a rare autosomal recessive disorder. The molecular nature of the disease is not fully understood and is considered to be one of the ectodermal dysplasia defects. In this report, we describe clinical, histologic, and ultrastructural features in two siblings born to consanguineous parents with a brief review of the literature.

Authors+Show Affiliations

As'ad Al-Hamad Dermatology Center, Al-Sabah Hospital, Kuwait. artinanda@hotmail.comNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article
Review

Language

eng

PubMed ID

20537066

Citation

Nanda, Arti, et al. "GAPO Syndrome: a Report of Two Siblings and a Review of Literature." Pediatric Dermatology, vol. 27, no. 2, 2010, pp. 156-61.
Nanda A, Al-Ateeqi WA, Al-Khawari MA, et al. GAPO syndrome: a report of two siblings and a review of literature. Pediatr Dermatol. 2010;27(2):156-61.
Nanda, A., Al-Ateeqi, W. A., Al-Khawari, M. A., Alsaleh, Q. A., & Anim, J. T. (2010). GAPO syndrome: a report of two siblings and a review of literature. Pediatric Dermatology, 27(2), 156-61. https://doi.org/10.1111/j.1525-1470.2010.01100.x
Nanda A, et al. GAPO Syndrome: a Report of Two Siblings and a Review of Literature. Pediatr Dermatol. 2010 Mar-Apr;27(2):156-61. PubMed PMID: 20537066.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - GAPO syndrome: a report of two siblings and a review of literature. AU - Nanda,Arti, AU - Al-Ateeqi,Wafa A, AU - Al-Khawari,Mona A, AU - Alsaleh,Qasem A, AU - Anim,Jeoram T, PY - 2010/6/12/entrez PY - 2010/6/12/pubmed PY - 2010/9/29/medline SP - 156 EP - 61 JF - Pediatric dermatology JO - Pediatr Dermatol VL - 27 IS - 2 N2 - Growth retardation, alopecia, pseudoanodontia, optic atrophy (GAPO) syndrome is a rare autosomal recessive disorder. The molecular nature of the disease is not fully understood and is considered to be one of the ectodermal dysplasia defects. In this report, we describe clinical, histologic, and ultrastructural features in two siblings born to consanguineous parents with a brief review of the literature. SN - 1525-1470 UR - https://www.unboundmedicine.com/medline/citation/20537066/GAPO_syndrome:_a_report_of_two_siblings_and_a_review_of_literature_ L2 - https://doi.org/10.1111/j.1525-1470.2010.01100.x DB - PRIME DP - Unbound Medicine ER -