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Published in: Skeletal Radiology 10/2007

01-10-2007 | Case Report

Berardinelli-Seip lipodystrophy

Authors: Yuko Kobashi, Amy Schoenbaum, Robert P. Hasserjian, Daniel I. Rosenthal

Published in: Skeletal Radiology | Issue 10/2007

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Abstract

Berardinelli-Seip lipodystrophy (BSCL) is a rare, but widely distributed, congenital disorder of metabolism. It is characterized by insulin-resistant diabetes mellitus and marked deficiency of adipose tissue. The clinical and imaging features of the syndrome are mostly due to fat deficiency, diabetes, or to manifestations of secondary hyperinsulinemia, which results from the failure of the tissues to respond to insulin. Absence of fat may be generalized, or depending upon the subtype of the disease, may not affect areas where fat plays a mechanical function, such as the palms and soles. Muscles appear hypertrophic. In addition, characteristic, but idiopathic, peri-articular lytic lesions may be seen in some individuals. The combination of imaging, clinical, and laboratory findings is characteristic and readily recognized once the components of the syndrome are known.
Literature
1.
go back to reference Berardinelli W. An undiagnosed endocrinometabolic syndrome: report of two cases [abstract]. J Clin Endocr 1954; 14: 193–204.PubMedCrossRef Berardinelli W. An undiagnosed endocrinometabolic syndrome: report of two cases [abstract]. J Clin Endocr 1954; 14: 193–204.PubMedCrossRef
2.
go back to reference Seip M. Lipodystrophy and gigantism with associated endocrine manifestation: a new diencephalic syndrome? [abstract] Acta Paediatr 1959; 48: 555–574.PubMed Seip M. Lipodystrophy and gigantism with associated endocrine manifestation: a new diencephalic syndrome? [abstract] Acta Paediatr 1959; 48: 555–574.PubMed
3.
go back to reference Mandal K, Aneja S, Khan A. Berardinelli-Seip congenital lipodystrophy [abstract]. Indian Pediatr 2006; 43: 440–445.PubMed Mandal K, Aneja S, Khan A. Berardinelli-Seip congenital lipodystrophy [abstract]. Indian Pediatr 2006; 43: 440–445.PubMed
4.
5.
go back to reference Brunzell JD, Shankle SW, Bethune JE. Congenital generalized lipodystrophy and systemic cystic angiomatosis: the simultaneous occurrence of two unusual syndromes in a single family [abstract]. Ann Intern Med 1968; 69: 501–516.PubMed Brunzell JD, Shankle SW, Bethune JE. Congenital generalized lipodystrophy and systemic cystic angiomatosis: the simultaneous occurrence of two unusual syndromes in a single family [abstract]. Ann Intern Med 1968; 69: 501–516.PubMed
6.
go back to reference Garg A, Wilson R, Arioglu E, Zaida Z, Gurakan F, et al. A gene for congenital generalized lipodystrophy maps to human chromosome 9q34 [abstract]. J Clin Endocr Metab 1999; 84:3390–3394.PubMedCrossRef Garg A, Wilson R, Arioglu E, Zaida Z, Gurakan F, et al. A gene for congenital generalized lipodystrophy maps to human chromosome 9q34 [abstract]. J Clin Endocr Metab 1999; 84:3390–3394.PubMedCrossRef
7.
go back to reference Van Maldergem L, Magre J, Khallouf TE, Gedde-Dahl T, Delepine M, Trygstad O. Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy [abstract]. J Med Genet 2002; 39: 722–733.PubMedCrossRef Van Maldergem L, Magre J, Khallouf TE, Gedde-Dahl T, Delepine M, Trygstad O. Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy [abstract]. J Med Genet 2002; 39: 722–733.PubMedCrossRef
8.
go back to reference Simha V, Garg A. Phenotypic heterogeneity in body fat distribution in patients with congenital generalized lipodystrophy caused by mutations in the AGPAT2 or Seipin genes [abstract]. J Clin Endocr Metab 2003; 88: 5433–5437.PubMedCrossRef Simha V, Garg A. Phenotypic heterogeneity in body fat distribution in patients with congenital generalized lipodystrophy caused by mutations in the AGPAT2 or Seipin genes [abstract]. J Clin Endocr Metab 2003; 88: 5433–5437.PubMedCrossRef
9.
go back to reference Schwartz MW, Porte D Jr. Diabetes, obesity, and the brain [abstract]. Science 2005; 307: 375–379.PubMedCrossRef Schwartz MW, Porte D Jr. Diabetes, obesity, and the brain [abstract]. Science 2005; 307: 375–379.PubMedCrossRef
10.
go back to reference Seaman JP, Kjeldsberg CR, Linker A. Gelatinous transformation of the bone marrow. Hum Pathol 1978; 9: 685–692.PubMedCrossRef Seaman JP, Kjeldsberg CR, Linker A. Gelatinous transformation of the bone marrow. Hum Pathol 1978; 9: 685–692.PubMedCrossRef
11.
go back to reference Tins B, Cassar-Pullicino V. Marrow changes in anorexia nervosa masking the presence of stress fractures on MR imaging. Skeletal Radiol 2006; 35: 857–860.PubMedCrossRef Tins B, Cassar-Pullicino V. Marrow changes in anorexia nervosa masking the presence of stress fractures on MR imaging. Skeletal Radiol 2006; 35: 857–860.PubMedCrossRef
13.
go back to reference Hegele R. Atherosclerosis associated with monogenic insulin resistance [abstract]. Circulation 2001; 103: 2225–2229.PubMed Hegele R. Atherosclerosis associated with monogenic insulin resistance [abstract]. Circulation 2001; 103: 2225–2229.PubMed
14.
go back to reference Oral EA, Simha V, Ruiz E, et al. Leptin-replacement therapy for lipodystrophy [abstract]. N Engl J Med 2002; 346: 570–578.PubMedCrossRef Oral EA, Simha V, Ruiz E, et al. Leptin-replacement therapy for lipodystrophy [abstract]. N Engl J Med 2002; 346: 570–578.PubMedCrossRef
Metadata
Title
Berardinelli-Seip lipodystrophy
Authors
Yuko Kobashi
Amy Schoenbaum
Robert P. Hasserjian
Daniel I. Rosenthal
Publication date
01-10-2007
Publisher
Springer-Verlag
Published in
Skeletal Radiology / Issue 10/2007
Print ISSN: 0364-2348
Electronic ISSN: 1432-2161
DOI
https://doi.org/10.1007/s00256-007-0332-4

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