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5p15.2 Google OMIM Orphanet PubMed Wikipedia Cri-du-chat syndrome *Gene map locus 5p15.2 Cat cry syndrome Deletion 5p [Clinical features: microcephaly; round face; hypertelorism; micrognathia; prominent nasal bridge; epicanthic folds; hypotonia; severe psychomotor retardation] [Inheritance: most cases are the result of de novo deletions] |
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Reversal of bronchiectasis caused by chronic aspiration in cri du chat syndrome |
Cri-du-chat Syndrome |
Cri-du-chat Syndrome |
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Archives of Disease in Childhood |
eMedicine |
eMedicine |
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Cri du Chat syndrome |
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Orphanet Journal of Rare Diseases |
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Edited by Aldo Campana,
August 21, 2012
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