Congenital generalized lipodystrophy: A case report with neurological involvement;Lipodystrophie congénitale généralisée de type 1 avec atteinte neurologique

Archives de Pediatrie

Volumn 16, Issue 1, 2009, Pages 27-31

  Ben Turkia, H ^a   Tebib, N ^a   Azzouz, H ^a   Slim Abdelmoula, M ^a   Ben Chehida, A ^a   Hubert, P ^b   Douira, W ^c   Ben Dridi, M F ^a  

^a LA RABTA HOSPITAL   (Tunisia)

^b INSTITUTE OF PATHOLOGY AND GENETICS   (Belgium)

^c CHILDREN S HOSPITAL   (Tunisia)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHILD; GENE MUTATION; GENOTYPE; HEPATOMEGALY; HOMOZYGOTE; HUMAN; HYPERINSULINEMIA; HYPERMETABOLISM; HYPERTROPHIC CARDIOMYOPATHY; INSULIN RESISTANCE; LIBYAN ARAB JAMAHIRIYA; LIPODYSTROPHY; MUSCLE HYPERTONIA; MUSCLE HYPERTROPHY; NEUROLOGIC DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; WHITE MATTER;

ADOLESCENT; AGE FACTORS; BRAIN DISEASES; CHILD; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; FEMALE; FOLLOW-UP STUDIES; GENOTYPE; HOMOZYGOTE; HUMANS; INFANT; INFANT, NEWBORN; INSULIN RESISTANCE; LIPODYSTROPHY, CONGENITAL GENERALIZED; MAGNETIC RESONANCE IMAGING; MUTATION; PHENOTYPE; TIME FACTORS; TREATMENT OUTCOME;

EID: 58149305958     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.arcped.2008.10.005     Document Type: Article

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