Literature DB >> 7502362

Congenital generalized lipodystrophy: Berardinelli syndrome. Report of two siblings.

F Gürakan1, N Koçak, A Yüce.   

Abstract

Two successively born infants with Berardinelli syndrome, an unusual lipodystrophic disease, are reported. In addition to hepatomegaly, accelerated growth, muscle hypertrophy, lack of adipose tissue, hirsutism and hypertriglyceridemia, which are the characteristics of the syndrome, these brothers demonstrated bilateral, symmetrical, renal medullary hyperechogenicity, which has not before been reported in association with generalized lipodystrophy. Although more than 25 cases have been recorded, the metabolic defect responsible for this inborn error of metabolism has not yet been determined.

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Year:  1995        PMID: 7502362

Source DB:  PubMed          Journal:  Turk J Pediatr        ISSN: 0041-4301            Impact factor:   0.552


  1 in total

1.  Natural History of Congenital Generalized Lipodystrophy: A Nationwide Study From Turkey.

Authors:  Baris Akinci; Huseyin Onay; Tevfik Demir; Samim Ozen; Hulya Kayserili; Gulcin Akinci; Banu Nur; Beyhan Tuysuz; Mehmet Nuri Ozbek; Adem Gungor; Ilgin Yildirim Simsir; Canan Altay; Leyla Demir; Enver Simsek; Murat Atmaca; Haluk Topaloglu; Habib Bilen; Hulusi Atmaca; Tahir Atik; Umit Cavdar; Umut Altunoglu; Ayca Aslanger; Ercan Mihci; Mustafa Secil; Fusun Saygili; Abdurrahman Comlekci; Abhimanyu Garg
Journal:  J Clin Endocrinol Metab       Date:  2016-05-04       Impact factor: 5.958

  1 in total

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