Literature DB >> 35769959

Wolman's Disease: A Rare Cause of Infantile Cholestasis and Cirrhosis.

Jagadeesh Menon1, Naresh Shanmugam1, Sripriya Srinivas2, Mukul Vij3, Anil Jalan4, Mettu Srinivas Reddy5, Mohamed Rela5,6.   

Abstract

Liver cirrhosis in infancy can be secondary to various etiologies such as biliary atresia, familial cholestatic and metabolic disorders. Wolman's disease (WD) is a lysosomal storage disorder caused by the absence of lysosomal acid lipase enzyme activity and a significant association with infantile cholestasis and cirrhosis. We encountered an infant presenting with advanced cirrhosis and decompensation having splenomegaly for which the underlying etiology was found to be WD and the diagnostic clue came from abdominal X-ray showing bilateral adrenal calcifications. The diagnosis was confirmed by genetic analysis. The outcome was poor and died before 6 months of age without enzyme replacement therapy or hematopoietic stem cell transplantation. Thieme. All rights reserved.

Entities:  

Keywords:  Wolman's disease; adrenal calcification; cirrhosis; infantile cholestasis

Year:  2020        PMID: 35769959      PMCID: PMC9236733          DOI: 10.1055/s-0040-1715119

Source DB:  PubMed          Journal:  J Pediatr Genet        ISSN: 2146-460X


  10 in total

1.  Primary familial xanthomatosis with involvement and calcification of the adrenals. Report of two more cases in siblings of a previously described infant.

Authors:  M WOLMAN; V V STERK; S GATT; M FRENKEL
Journal:  Pediatrics       Date:  1961-11       Impact factor: 7.124

2.  A rare constellation of imaging findings in Wolman disease.

Authors:  Debraj Sen; Lovleen Satija; Sudhir Saxena; Vikas Rastogi; Meenu Singh
Journal:  Med J Armed Forces India       Date:  2014-04-26

Review 3.  Lysosomal acid lipase deficiency allograft recurrence and liver failure- clinical outcomes of 18 liver transplantation patients.

Authors:  Donna Lee Bernstein; Steven Lobritto; Alina Iuga; Helen Remotti; Thomas Schiano; Maria Isabel Fiel; Manisha Balwani
Journal:  Mol Genet Metab       Date:  2018-03-27       Impact factor: 4.797

4.  Extended use of a selective inhibitor of acid lipase for the diagnosis of Wolman disease and cholesteryl ester storage disease.

Authors:  G Civallero; J De Mari; C Bittar; M Burin; R Giugliani
Journal:  Gene       Date:  2014-02-06       Impact factor: 3.688

Review 5.  Wolman's disease and cholesteryl ester storage disorder: the phenotypic spectrum of lysosomal acid lipase deficiency.

Authors:  Marinos Pericleous; Claire Kelly; Tim Wang; Callum Livingstone; Aftab Ala
Journal:  Lancet Gastroenterol Hepatol       Date:  2017-09

6.  Niemann-Pick disease type C: diagnosis and outcome in children, with particular reference to liver disease.

Authors:  D A Kelly; B Portmann; A P Mowat; S Sherlock; B D Lake
Journal:  J Pediatr       Date:  1993-08       Impact factor: 4.406

7.  Survival in infants treated with sebelipase Alfa for lysosomal acid lipase deficiency: an open-label, multicenter, dose-escalation study.

Authors:  Simon A Jones; Sandra Rojas-Caro; Anthony G Quinn; Mark Friedman; Sachin Marulkar; Fatih Ezgu; Osama Zaki; J Jay Gargus; Joanne Hughes; Dominique Plantaz; Roshni Vara; Stephen Eckert; Jean-Baptiste Arnoux; Anais Brassier; Kim-Hanh Le Quan Sang; Vassili Valayannopoulos
Journal:  Orphanet J Rare Dis       Date:  2017-02-08       Impact factor: 4.123

8.  Clinical and genetic characterization of a Chanarin Dorfman Syndrome patient born to diseased parents.

Authors:  Murat Durdu; Sara Missaglia; Laura Moro; Daniela Tavian
Journal:  BMC Med Genet       Date:  2018-05-29       Impact factor: 2.103

Review 9.  Diagnosis and treatment of congenital tuberculosis: a systematic review of 92 cases.

Authors:  Chaofeng Li; Lili Liu; Yuhong Tao
Journal:  Orphanet J Rare Dis       Date:  2019-06-10       Impact factor: 4.123

10.  Rapid progression and mortality of lysosomal acid lipase deficiency presenting in infants.

Authors:  Simon A Jones; Vassili Valayannopoulos; Eugene Schneider; Stephen Eckert; Maryam Banikazemi; Martin Bialer; Stephen Cederbaum; Alicia Chan; Anil Dhawan; Maja Di Rocco; Jennifer Domm; Gregory M Enns; David Finegold; J Jay Gargus; Ornella Guardamagna; Christian Hendriksz; Iman G Mahmoud; Julian Raiman; Laila A Selim; Chester B Whitley; Osama Zaki; Anthony G Quinn
Journal:  Genet Med       Date:  2015-08-27       Impact factor: 8.822

  10 in total

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