Long-Term Course of Lipoprotein Lipase (LPL) Deficiency Due to Homozygous LPLAritain a Patient with Recurrent Pancreatitis, Retained Glucose Tolerance, and Atherosclerosis | Zendy

Masaaki Kawashiri | Zendy; Toshinori Higashikata | Zendy; Mihoko Mizuno | Zendy; Mutsuko Takata | Zendy; Shoji Katsuda | Zendy; Kenji Miwa | Zendy; Tsuyoshi Nozue | Zendy; Atsushi Nohara | Zendy; Akihiro Inazu | Zendy; Junji Kobayashi | Zendy; Junji Koizumi | Zendy; Hiroshi Mabuchi | Zendy

Open Access

Long-Term Course of Lipoprotein Lipase (LPL) Deficiency Due to Homozygous LPL_Aritain a Patient with Recurrent Pancreatitis, Retained Glucose Tolerance, and Atherosclerosis

Author(s) -

Masaaki Kawashiri,

Toshinori Higashikata,

Mihoko Mizuno,

Mutsuko Takata,

Shoji Katsuda,

Kenji Miwa,

Tsuyoshi Nozue,

Atsushi Nohara,

Akihiro Inazu,

Junji Kobayashi,

Junji Koizumi,

Hiroshi Mabuchi

Publication year - 2005

Publication title -

the journal of clinical endocrinology and metabolism

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 2.206

H-Index - 353

eISSN - 1945-7197

pISSN - 0021-972X

DOI - 10.1210/jc.2005-1098

Subject(s) - medicine , lipoprotein lipase , acute pancreatitis , endocrinology , pancreatitis , context (archaeology) , gastroenterology , biology , adipose tissue , paleontology

Lipoprotein lipase (LPL) deficiency is a rare autosomal recessive disorder caused by LPL gene mutation and is characterized by severe hyperchylomicronemia. Patients with LPL deficiency suffer from the frequent recurrence of acute pancreatitis, but the underlying mechanisms are not fully understood.

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