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CATCH 22 Syndrome.

Yoshiyuki Yonehara·Takashi Nakatsuka·Shigeru Ichioka·Nozomu Sasaki·Toshiki Kobayashi
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Abstract

CATCH 22 syndrome is characterized by cardiac defects, abnormal facial features, thymic hypoplasia, cleft palate, and hypocalcemia. It results from a deletion within chromosome 22q11. This syndrome is not a simple disease. It includes DiGeorge syndrome, conotruncal anomaly face syndrome, and velocardiofacial syndrome. The authors report two cases of CATCH 22 syndrome.

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Abnormalities, MultipleChild, PreschoolChromosome DeletionChromosomes, Human, Pair 22Cleft PalateDiagnosis, DifferentialFaciesFemaleHeart Defects, CongenitalHumansHypocalcemiaInfant, NewbornSyndromeThymus GlandCase ReportsJournal Article

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Yoshiyuki Yonehara, Takashi Nakatsuka, Shigeru Ichioka, Nozomu Sasaki, Toshiki Kobayashi. 2002. CATCH 22 Syndrome.. https://doi.org/10.1097/00001665-200209000-00005

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