Congenital generalized lipodystrophy
Appearance
Congenital generalized lipodystrophy (also known as "Berardinelli–Seip syndrome") is a rare autosomal dominant skin condition, characterized by an extreme paucity of fat in the subcutaneous tissues.[1]: 495
Berardinelli-Seip congenital lipodystrophy is a rare autosomal recessive condition associating insulin resistance, absence of subcutaneous fat and muscular hypertrophy.[2]With characteristic features like hepatomegaly, accelerated growth, muscle hypertrophy, lack of adipose tissue, hirsutism and hypertriglyceridemia.[3]Common cardiovascular alterations related to this syndrome are cardiac hypertrophy and arterial hypertension.[4] and it is associated with metabolic syndrome.
See also
External Links
References
- ^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.
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(help)CS1 maint: multiple names: authors list (link) - ^ Friguls B, Coroleu W, del Alcazar R, Hilbert P, Van Maldergem L, Pintos-Morell G (2009). "Severe cardiac phenotype of Berardinelli-Seip congenital lipodystrophy in an infant with homozygous E189X BSCL2 mutation". Eur J Med Genet. 52 (1): 14–6. doi:10.1016/j.ejmg.2008.10.006. PMID 19041432. Retrieved 2009-03-04.
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: CS1 maint: multiple names: authors list (link) - ^ Gürakan F, Koçak N, Yüce A (1995). "Congenital generalized lipodystrophy: Berardinelli syndrome. Report of two siblings". Turk. J. Pediatr. 37 (3): 241–6. PMID 7502362.
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(help)CS1 maint: multiple names: authors list (link) - ^ Viégas RF, Diniz RV, Viégas TM, Lira EB, Almeida DR (2000). "Cardiac involvement in total generalized lipodystrophy (Berardinelli- Seip syndrome)". Arq. Bras. Cardiol. 75 (3): 243–8. PMID 11018810.
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