Heterogeneity for congenital generalized lipodystrophy in seventeen patients from Oman

American Journal of Medical Genetics

Volumn 110, Issue 3, 2002, Pages 219-225

  Rajab, Anna ^a,d   Heathcote, Kirsten ^c   Joshi, Surendra ^b   Jeffery, Steve ^c   Patton, Michael ^c  

^a MINISTRY OF HEALTH   (Oman)

^b SULTAN QABOOS UNIVERSITY HOSPITAL   (Oman)

^c ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

^d NONE   (Oman)

Author keywords

Advanced bone age; Beradinelli Seip syndrome; Cardiac complications; Congenital generalized lipodystrophy; Genetic heterogeniety; Muscle hypertrophy; Oman; Pyloric stenosis; Sudden death

Indexed keywords

ACANTHOSIS NIGRICANS; ADIPOSE TISSUE; ADOLESCENT; ARTICLE; BERARDINELLI SEIP CONGENITAL LIPODYSTROPHY; CARDIOMYOPATHY; CHILD; CHROMOSOME 11Q; CLINICAL ARTICLE; CONGENITAL DISORDER; DISEASE SEVERITY; EXERCISE TOLERANCE; FEMALE; GENE LOCATION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; HEART ARRHYTHMIA; HEPATOMEGALY; HOMOZYGOSITY; HUMAN; INFANT DISEASE; INSULIN METABOLISM; INSULIN RESISTANCE; LIPODYSTROPHY; MALE; MUSCLE HYPERTROPHY; MYOPATHY; NEWBORN; OMAN; PERCUSSION MYOXEDEMA; PRIORITY JOURNAL; PYLORUS STENOSIS; SYNDROME DELINEATION;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; GENETIC HETEROGENEITY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INFANT; INFANT, NEWBORN; LIPODYSTROPHY; MALE; MICROSATELLITE REPEATS; OMAN;

EID: 0036644298     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10437     Document Type: Article

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