Výsledky vyhledávání - "Fernanda Mendes Götze"

Akademický článek

Ceratose pilar e ulerythema ophryogenes em mulher com monossomia do braço curto do cromosomo 18 Keratosis pilaris and ulerythema ophryogenes in a woman with monosomy of the short arm of chromosome 18

Autor: Charles André Carvalho, André Vicente Esteves de Carvalho, Andrea Kiss, Giorgio Paskulin, Fernanda Mendes Götze

Publikováno v: Anais Brasileiros de Dermatologia, Vol 86, Iss 4, Pp 42-45 (2011)

A monossomia parcial do braço curto do cromosomo 18 (síndrome do 18p) caracteriza-se, principalmente, por atraso na aquisição da fala, retardo mental leve a moderado e baixa estatura. Relatamos o caso de uma paciente com esta síndrome associada

Externí odkaz: https://doaj.org/article/3a15acb3fabb40f3a1c1e6395fc16657

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Keratosis pilaris and ulerythema ophryogenes in a woman with monosomy of the short arm of chromosome 18

Autor: Charles André Carvalho, Giorgio Adriano Paskulin, Fernanda Mendes Götze, A. V. Carvalho, Andrea Kiss

Publikováno v: Anais Brasileiros de Dermatologia, Volume: 86, Issue: 4 Supplement 1, Pages: 42-45, Published: AUG 2011
Anais Brasileiros de Dermatologia v.86 n.4 suppl.1 2011
Anais brasileiros de dermatologia
Sociedade Brasileira de Dermatologia (SBD)
instacron:SBD

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e747d24a4171dd16050afef4e4bb8466
https://doi.org/10.1590/s0365-05962011000700010

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Keratosis pilaris and ulerythema ophryogenes in a woman with monosomy of the short arm of chromosome 18

Autor: Charles André, Carvalho, André Vicente Esteves de, Carvalho, Andrea, Kiss, Giorgio, Paskulin, Fernanda Mendes, Götze

Publikováno v: Anais brasileiros de dermatologia. 86(4 Suppl 1)

Partial monosomy of the short arm of chromosome 18 (18p- syndrome) is characterized mainly by speech delay, mild to moderate mental retardation and short stature. We describe a patient with the 18p- syndrome and widespread severe keratosis pilaris an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::457953dfa59c93c17add3c9765811134
https://pubmed.ncbi.nlm.nih.gov/22068768

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