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A Novel Homozygous LIPA Mutation in a Korean Child with Lysosomal Acid Lipase Deficiency

Patients with lysosomal acid lipase (LAL) deficiency and glycogen storage disease (GSD) demonstrated hepatomegaly and dyslipidemia. In our case, a 6-year-old boy presented with hepatosplenomegaly. At 3 years of age, GSD had been diagnosed by liver biopsy at another hospital. He showed elevated serum...

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Detalles Bibliográficos
Autores principales:	Kim, Kwang Yeon, Kim, Ju Whi, Lee, Kyung Jae, Park, Eunhyang, Kang, Gyeong Hoon, Choi, Young Hun, Kim, Woo Sun, Ko, Jung Min, Moon, Jin Soo, Ko, Jae Sung
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2017
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5750382/ https://www.ncbi.nlm.nih.gov/pubmed/29302509 http://dx.doi.org/10.5223/pghn.2017.20.4.263

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