Title of article :
Berardinelli-Seip syndrome type 2 - An Egyptian child
Author/Authors :
shawky, r.m. Ain Shams University - pediatric department, genetics unit, Egypt , gamal, r. Ain Shams University - pediatric department, genetics unit, Egypt , seifeldin, n.s. Ain-Shams University - dermatology and venereology department, Egypt
From page :
189
To page :
193
Abstract :
We report a 2.5. year old male,first in order of birth of first cousin consanguineous parents with the typical features of Berardinelli-Seip congenital lipodystrophy 2 (BSCL2) since birth with moderate mental retardation. He had generalized lipodystrophy with various dermatologic and systemic manifestations. The patient looked older than his age with the loss of buccal pad of fat,hypertrichosis mainly on the back and lower limbs,thick scalp hair,mild prognathism,large hands and feet with prominent joints and muscular hypertrophy. Acanthosis nigricans was evident over the neck and both axillae inspite of the normal level of sugar and insulin. The abdomen was markedly prominent with mild hepatosplenomegaly and enlarged external genitals. Echo-cardiography demonstrated cardiac hypertrophy. Triglyceride level was high with reduced high density lipoproteins (HDL). © 2014.
Keywords :
Acanthosis nigricans , Cardiac hypertrophy , Congenital lipodystrophy , Hirsutism , Muscular hypertrophy , Prominent abdomen
Journal title :
Egyptian Journal of Medical Human Genetics
Journal title :
Egyptian Journal of Medical Human Genetics
Record number :
2721166
Link To Document :
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