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Cri du chat syndrome: short arm B [5] partial monosomy syndrome

Book ID: 118535305
Publisher: Elsevier Science
Year: 1967
Tongue: English
Weight: 915 KB
Volume: 70
Category: Article
ISSN: 1097-6833
DOI: 10.1016/s0022-3476(67)80365-2

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"CRI DU CHAT" SYNDROME

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Partial monosomy 22 as the result of an

Partial monosomy 22 as the result of an unbalanced translocation 5:22 in a patient with cri-du-chat syndrome

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A 2-year-old boy with features suggestive of cri-du-chat syndrome had a complex karyotype: 45,XY,--22,5p--,t(5p:22q). Clinical symptoms were catlike cry in early infancy, severe mental and motor retardation, failure to thrive, hypertelorism, antimongoloid slant of the eyes, ptosis of the eyelids, ep

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Long arm measurements of chromosomes 4 a

Long arm measurements of chromosomes 4 and 5 with special reference to the cri du chat syndrome

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