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@article{554908,
author = {Litzman, Jiří and Bučková, Hana and Ventruba, Jiří and Holčíková, Alena and Mikyška, Pavel and Lokaj, Jindřich},
article_number = {7},
keywords = {Cutis laxa; Dandy-Walker syndrome; hypogammaglobulinemia; leukopenia; subclavian artery - abnormalities},
language = {eng},
issn = {0803-5253},
journal = {Acta Paediatrica},
note = {Cutis laxa, Dandy-Walker syndrome, hypogammaglobulinemia, leukopenia, subclavian artery - abnormalities},
title = {A concurrent occurrence of cutis laxa, Dandy-Walker syndrome and immunodeficiency in a girl},
volume = {92},
year = {2003}
}
TY - JOUR
ID - 554908
AU - Litzman, Jiří - Bučková, Hana - Ventruba, Jiří - Holčíková, Alena - Mikyška, Pavel - Lokaj, Jindřich
PY - 2003
TI - A concurrent occurrence of cutis laxa, Dandy-Walker syndrome and immunodeficiency in a girl
JF - Acta Paediatrica
VL - 92
IS - 7
SP - 861-864
EP - 861-864
SN - 08035253
N1 - Cutis laxa, Dandy-Walker syndrome, hypogammaglobulinemia, leukopenia, subclavian artery - abnormalities
KW - Cutis laxa
KW - Dandy-Walker syndrome
KW - hypogammaglobulinemia
KW - leukopenia
KW - subclavian artery - abnormalities
N2 - We report on a 17-year-old girl with inherited cutis laxa, immunodeficiency and Dandy-Walker syndrome. Immunodeficiency manifested itself by decreased and fluctuating levels of IgG, IgA and IgM and intermittent leukopenia causing increased susceptibility to respiratory tract infections. Dandy-Walker syndrome (agenesis of the cerebellar vermis with a large posterior fossa cyst communicating with an enlarged 4th ventricle) was demonstrated by a CT scan, but with the exception of macrocrania no typical signs or symptoms were observed at the age of 17. A loose hyperextensible skin with pendulous skin folds as a manifestation of cutis laxa was observed from birth. Anomalies of the right pulmonary artery, abnormal branching of the left arteria subclavia (arteria lusoria) from the left aortic arch and bicuspidal aortic valve were also present. To the knowledge of the authors this combination of relatively rare diseases has not been reported yet.
ER -
LITZMAN, Jiří, Hana BUČKOVÁ, Jiří VENTRUBA, Alena HOLČÍKOVÁ, Pavel MIKYŠKA a Jindřich LOKAJ. A concurrent occurrence of cutis laxa, Dandy-Walker syndrome and immunodeficiency in a girl. Online. \textit{Acta Paediatrica}. 2003, roč.~92, č.~7, s.~861-864. ISSN~0803-5253. [citováno 2024-04-24]
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