Lysosomal acid lipase deficiency in all siblings of the same parents.

Maciejko, James J; Anne, Premchand; Raza, Saleem; Lyons, Hernando J

Maciejko, James J; Anne, Premchand; Raza, Saleem; Lyons, Hernando J.

Affiliation

Maciejko JJ; Division of Cardiology, Department of Internal Medicine, St. John Hospital and Medical Center, and Wayne State University School of Medicine, Department of Internal Medicine, Detroit, MI, USA. Electronic address: james.maciejko@stjohn.org.
Anne P; Department of Pediatrics, St. John Providence Children's Hospital, and Wayne State University School of Medicine, Department of Pediatrics, Detroit, MI, USA.
Raza S; Department of Pediatrics, St. John Providence Children's Hospital, and Wayne State University School of Medicine, Department of Pediatrics, Detroit, MI, USA.
Lyons HJ; Department of Pediatrics, St. John Providence Children's Hospital, and Wayne State University School of Medicine, Department of Pediatrics, Detroit, MI, USA.

J Clin Lipidol ; 11(2): 567-574, 2017.

Article in En | MEDLINE | ID: mdl-28502515

Subject(s)

Parents; Siblings; Wolman Disease/genetics; Adolescent; Adult; Child; Female; Heterozygote; Humans; Male; Mutation; Pedigree; Wolman Disease/pathology; Wolman Disease/physiopathology; Young Adult; Wolman Disease

Key words

Hepatic enzyme elevation; Hyperlipidemia; LIPA gene; Lysosomal acid lipase deficiency; Sebelipase alfa

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parents / Wolman Disease / Siblings Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Female / Humans / Male Language: En Journal: J Clin Lipidol Journal subject: BIOQUIMICA / METABOLISMO Year: 2017 Document type: Article Country of publication: United States

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