Literature DB >> 23357145

A three month-old infant with severe hyperchylomicronemia: molecular diagnosis and extracorporeal treatment.

Claudia Stefanutti1, Maria Gozzer, Livia Pisciotta, Patrizia D'Eufemia, Giovanna Bosco, Claudia Morozzi, Francesco Papadia, Manhaz Shafii, Serafina Di Giacomo, Stefano Bertolini.   

Abstract

OBJECTIVE: Chylomicronemia syndrome presenting in childhood is a rare recessive disorder due to mutations of lipoprotein lipase (LPL) and more rarely of APOC2, APOA5, GPIHBP1 or LMF1 genes. It often requires urgent and suitable treatment to avoid acute pancreatitis. The aim of this study was the molecular characterization and treatment of a 3 month-old infant with plasma triglycerides (TG) > 300 mmol/L.
METHODS: All candidate genes were sequenced. The patient was submitted to one plasma-exchange (PEX) procedure and subsequently to a rigid lipid-lowering diet (milk: Monogen(®)).
RESULTS: The proband was homozygous for a novel LPL mutation (c.242G > A, p.G81D) which in silico results pathogenic. After PEX, which was well tolerated, TG dropped to 64 mmol/L. During 5-month follow-up there was a clear trend towards lower and stable TG values.
CONCLUSION: PEX is applicable in subjects with very low body weight when the extreme severity of the clinical picture has no therapeutic alternatives.
Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.

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Year:  2013        PMID: 23357145     DOI: 10.1016/j.atherosclerosissup.2012.10.020

Source DB:  PubMed          Journal:  Atheroscler Suppl        ISSN: 1567-5688            Impact factor:   3.235


  10 in total

Review 1.  Chylomicronaemia--current diagnosis and future therapies.

Authors:  Amanda J Brahm; Robert A Hegele
Journal:  Nat Rev Endocrinol       Date:  2015-03-03       Impact factor: 43.330

2.  Severe hypertriglyceridemia in a newborn with monogenic lipoprotein lipase deficiency: an unconventional therapeutic approach with exchange transfusion.

Authors:  Lorenza Pugni; Enrica Riva; Carlo Pietrasanta; Claudio Rabacchi; Stefano Bertolini; Cristina Pederiva; Fabio Mosca; Sebastiano Calandra
Journal:  JIMD Rep       Date:  2013-10-20

3.  Rare LPL gene missense mutation in an infant with hypertriglyceridemia.

Authors:  Yuan-Yuan Qin; Ai-Qiu Wei; Qing-Wen Shan; Xiao-Ying Xian; Yang-Yang Wu; Lin Liao; Jie Yan; Zhan-Feng Lai; Fa-Quan Lin
Journal:  J Clin Lab Anal       Date:  2018-02-25       Impact factor: 2.352

4.  Clinical, biochemical and molecular analysis of two infants with familial chylomicronemia syndrome.

Authors:  Yonghong Zhang; Jing Zhou; Wenxin Zheng; Zhangzhang Lan; Zhiwei Huang; Qingnan Yang; Chengbo Liu; Rui Gao; Yongjun Zhang
Journal:  Lipids Health Dis       Date:  2016-05-06       Impact factor: 3.876

5.  A 1-month-old infant with chylomicronemia due to GPIHBP1 gene mutation treated by plasmapheresis.

Authors:  Mo Kyung Jung; Juhyun Jin; Hyun Ok Kim; Ahreum Kwon; Hyun Wook Chae; Seok Jin Kang; Duk Hee Kim; Ho-Seong Kim
Journal:  Ann Pediatr Endocrinol Metab       Date:  2017-03-31

6.  Management strategy and novel ophthalmological findings in neonatal severe hypertriglyceridemia: a case report and literature review.

Authors:  Nehal M El-Koofy; Yasmeen A Abdo; Dina El-Fayoumi; Amanne F Esmael; Mohamed A Elmonem; Zahraa Ezzeldin
Journal:  Lipids Health Dis       Date:  2021-04-20       Impact factor: 3.876

7.  Case Report: Successful Management of a 29-Day-Old Infant With Severe Hyperlipidemia From a Novel Homozygous Variant of GPIHBP1 Gene.

Authors:  Shu Liu; Zhiqing Wang; Xianhua Zheng; Ye Zhang; Sisi Wei; Haimei OuYang; Jinqun Liang; Nuan Chen; Weihong Zeng; Jianhui Jiang
Journal:  Front Pediatr       Date:  2022-03-10       Impact factor: 3.418

Review 8.  Causes, clinical findings and therapeutic options in chylomicronemia syndrome, a special form of hypertriglyceridemia.

Authors:  György Paragh; Ákos Németh; Mariann Harangi; Maciej Banach; Péter Fülöp
Journal:  Lipids Health Dis       Date:  2022-02-10       Impact factor: 3.876

9.  Plasma exchange therapy for familial chylomicronemia syndrome in infant: A case report.

Authors:  Lei Han; Guangfeng Qiang; Lei Yang; Rui Kou; Qiubo Li; Meiyun Xin; Ruihan Liu; Zhengjun Zhang
Journal:  Medicine (Baltimore)       Date:  2022-08-12       Impact factor: 1.817

Review 10.  Genetic-based prediction of disease traits: prediction is very difficult, especially about the future.

Authors:  Steven J Schrodi; Shubhabrata Mukherjee; Ying Shan; Gerard Tromp; John J Sninsky; Amy P Callear; Tonia C Carter; Zhan Ye; Jonathan L Haines; Murray H Brilliant; Paul K Crane; Diane T Smelser; Robert C Elston; Daniel E Weeks
Journal:  Front Genet       Date:  2014-06-02       Impact factor: 4.599

  10 in total

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