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CHARGE Syndrome Includes Hypogonadotropic Hypogonadism and Abnormal Olfactory Bulb Development
Author(s) -
Graziella Pinto,
Véronique Abadie,
Robin Mesnage,
J. Blustajn,
S Cabrol,
Jeanne Amiel,
Lucie HertzPannier,
A.-M. Bertrand,
Stanislas Lyonnet,
Rebecca Rappaport,
Irène Netchine
Publication year - 2005
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2004-2474
Subject(s) - charge syndrome , choanal atresia , hypoplasia , context (archaeology) , coloboma , hypogonadotropic hypogonadism , olfactory bulb , cerebellar hypoplasia (non human) , medicine , atresia , anosmia , anatomy , endocrinology , biology , central nervous system , hormone , disease , covid-19 , psychiatry , infectious disease (medical specialty) , paleontology , cerebellum
CHARGE (coloboma, heart defect, choanal atresia, retarded growth and development, genital hypoplasia, ear abnormalities, and/or hearing loss defect) syndrome consists of a combination of congenital malformations including genital hypoplasia and retarded growth.

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