Kenny-Caffey syndrome: An Arab variant?

Clinical Genetics

Volumn 55, Issue 1, 1999, Pages 44-49

  Sabry, M A ^b   Farag, T I ^a   Shaltout, A A ^b   Zaki, M ^b   Al Mazidi, Z ^b   Abulhassan, S J ^b   Al Torki, N ^b   Quishawi, A ^b   Al Awadi, S A ^b  

^a DALHOUSIE UNIVERSITY   (Canada)

^b NONE

Author keywords

Dwarfism; Episodic hypocalcemia; Kenny Caffey syndrome

Indexed keywords

ARAB; ARTICLE; CASE REPORT; CHROMOSOME 10P; CHROMOSOME 22Q; CLINICAL FEATURE; DWARFISM; FEMALE; GENE DELETION; GENETIC HETEROGENEITY; HUMAN; HYPOCALCEMIA; HYPOPARATHYROIDISM; MENTAL DEFICIENCY; MICROCEPHALY; PHENOTYPE; PRIORITY JOURNAL; PSYCHOMOTOR RETARDATION; SEIZURE; SHORT STATURE;

ABNORMALITIES, MULTIPLE; ARABS; BONE AND BONES; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 22; DEVELOPMENTAL DISABILITIES; EYE ABNORMALITIES; FEMALE; GENE DELETION; GENETIC HETEROGENEITY; HUMANS; HYPOPARATHYROIDISM; MENTAL RETARDATION; MICROCEPHALY; PSYCHOMOTOR DISORDERS; SEIZURES; SYNDROME;

EID: 0032903371     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.1999.550108.x     Document Type: Article

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