[Williams-Beuren syndrome in combination with celiac disease]

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[Williams-Beuren syndrome in combination with celiac disease]. / Pankau, R; Partsch, C J; Gosch, A; Santer, René.

in: MONATSSCHR KINDERH, Jahrgang 141, Nr. 7, 7, 1993, S. 577-580.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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@article{e248785d206243fa96bd0496011f1c0e,
title = "[Williams-Beuren syndrome in combination with celiac disease]",
abstract = "At age 5 years coeliac disease was diagnosed in a boy with Williams-Beuren syndrome. Gastrointestinal symptoms may be similar in both disorders. Short stature, not only in comparison to the normal population but also in comparison to syndrome-specific growth standards, and failure to thrive led to the diagnosis coeliac disease. During the first year of dietetic therapy the boy showed marked weight gain, catch-up growth and a normalisation of red blood count. Gliadin-IgG antibodies and endomysium-IgA antibodies who were positive before treatment were no longer detectable. Our case demonstrates that syndrome-specific growth standards are helpful even though the combination of Williams-Beuren syndrome with a second disorder is very unlikely (Williams-Beuren syndrome and coeliac disease are to be expected in 1:13.7-1:25 millions).",
author = "R Pankau and Partsch, {C J} and A Gosch and Ren{\'e} Santer",
year = "1993",
language = "Deutsch",
volume = "141",
pages = "577--580",
journal = "MONATSSCHR KINDERH",
issn = "0026-9298",
publisher = "Springer",
number = "7",

}

RIS

TY - JOUR

T1 - [Williams-Beuren syndrome in combination with celiac disease]

AU - Pankau, R

AU - Partsch, C J

AU - Gosch, A

AU - Santer, René

PY - 1993

Y1 - 1993

N2 - At age 5 years coeliac disease was diagnosed in a boy with Williams-Beuren syndrome. Gastrointestinal symptoms may be similar in both disorders. Short stature, not only in comparison to the normal population but also in comparison to syndrome-specific growth standards, and failure to thrive led to the diagnosis coeliac disease. During the first year of dietetic therapy the boy showed marked weight gain, catch-up growth and a normalisation of red blood count. Gliadin-IgG antibodies and endomysium-IgA antibodies who were positive before treatment were no longer detectable. Our case demonstrates that syndrome-specific growth standards are helpful even though the combination of Williams-Beuren syndrome with a second disorder is very unlikely (Williams-Beuren syndrome and coeliac disease are to be expected in 1:13.7-1:25 millions).

AB - At age 5 years coeliac disease was diagnosed in a boy with Williams-Beuren syndrome. Gastrointestinal symptoms may be similar in both disorders. Short stature, not only in comparison to the normal population but also in comparison to syndrome-specific growth standards, and failure to thrive led to the diagnosis coeliac disease. During the first year of dietetic therapy the boy showed marked weight gain, catch-up growth and a normalisation of red blood count. Gliadin-IgG antibodies and endomysium-IgA antibodies who were positive before treatment were no longer detectable. Our case demonstrates that syndrome-specific growth standards are helpful even though the combination of Williams-Beuren syndrome with a second disorder is very unlikely (Williams-Beuren syndrome and coeliac disease are to be expected in 1:13.7-1:25 millions).

M3 - SCORING: Zeitschriftenaufsatz

VL - 141

SP - 577

EP - 580

JO - MONATSSCHR KINDERH

JF - MONATSSCHR KINDERH

SN - 0026-9298

IS - 7

M1 - 7

ER -