Literature DB >> 24063868

Abnormal fat distribution in PMM2-CDG.

D F G J Wolthuis1, E V van Asbeck, T Kozicz, E Morava.   

Abstract

We hypothesize that abnormal fat distribution, a common feature of PMM2-CDG, is associated with abnormal perinatal hormone regulation. We assessed 32 cases with PMM2-CDG, for the comorbidity of hypoglycemia/hyperinsulinism and fat pads. Ninety percent of patients with hypoketotic hypoglycemia and/or hyperinsulinism had abnormal fat distribution, while normoglycemic patients showed this feature in 50% of the cases. This statistically significant difference suggests an etiological role of the insulin receptor in developing abnormal fat distribution in PMM2-CDG.
© 2013.

Entities:  

Keywords:  Abnormal fat distribution; Congenital disorders of glycosylation; Hypoglycemia; PMM2-CDG

Mesh:

Substances:

Year:  2013        PMID: 24063868     DOI: 10.1016/j.ymgme.2013.08.017

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  5 in total

Review 1.  Recognizable phenotypes in CDG.

Authors:  Carlos R Ferreira; Ruqaia Altassan; Dorinda Marques-Da-Silva; Rita Francisco; Jaak Jaeken; Eva Morava
Journal:  J Inherit Metab Dis       Date:  2018-04-13       Impact factor: 4.982

2.  Hypoglycemia in CDG patients due to PMM2 mutations: Follow up on hyperinsulinemic patients.

Authors:  Hossein Moravej; Ruqaiah Altassan; Jaak Jaeken; Gregory M Enns; Carolyn Ellaway; Shanti Balasubramaniam; Pascale De Lonlay; David Coman; Saadet Mercimek-Andrews; Peter Witters; Eva Morava
Journal:  JIMD Rep       Date:  2019-11-25

3.  Classical Galactosaemia and CDG, the N-Glycosylation Interface. A Review.

Authors:  Ashwini Maratha; Hugh-Owen Colhoun; Ina Knerr; Karen P Coss; Peter Doran; Eileen P Treacy
Journal:  JIMD Rep       Date:  2016-08-09

Review 4.  Inborn errors of metabolism associated with hyperglycaemic ketoacidosis and diabetes mellitus: narrative review.

Authors:  Majid Alfadhel; Amir Babiker
Journal:  Sudan J Paediatr       Date:  2018

5.  Clinical and whole-exome sequencing findings in two siblings from Hani ethnic minority with congenital glycosylation disorders.

Authors:  Zhen Zhang; Ti-Long Huang; Jing Ma; Wen-Ji He; Huaiyu Gu
Journal:  BMC Med Genet       Date:  2019-11-14       Impact factor: 2.103

  5 in total

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