Literature DB >> 28915122

Understanding fetal factors that contribute to preterm birth: Sjögren-Larsson syndrome as a model.

Pippa Staps1, Marije Hogeveen2, Joris Fuijkschot2, Joris van Drongelen3, Michèl A A P Willemsen1.   

Abstract

AIM: Preterm birth is the world's leading cause of neonatal death. Unfortunately, the pathophysiology of preterm birth remains poorly understood. Sjögren-Larsson syndrome is a rare, neurometabolic disorder caused by a fatty aldehyde dehydrogenase deficiency. A majority of patients with Sjögren-Larsson syndrome is born preterm.
METHODS: Data of all known Dutch patients with Sjögren-Larsson syndrome and all cases reported in literature were analyzed to learn from preterm birth in context of this rare disease.
RESULTS: Exact gestational age was known in 33 Dutch patients; 24 (73%) of them were born preterm, with a median gestational age of 36 weeks. The literature search confirmed our findings: 13 (59%) of 22 cases was born preterm.
CONCLUSIONS: Preterm birth is a hallmark of Sjögren-Larsson syndrome, presumably caused by the abnormal lipid metabolism of the fetus. At least five additional rare genetic disorders (namely Ehlers-Danlos syndrome, ichthyosis prematurity syndrome, congenital analbuminemia, osteogenesis imperfecta type II and restrictive dermopathy) were found in literature that lead to preterm birth of the affected fetus. These disorders are in fact "experiments of nature" and as such they shed new lights on the mechanisms causing preterm birth.

Entities:  

Keywords:  Genetics; Sjögren-Larsson syndrome; genetic diseases; inborn; physiopathology; preterm birth

Mesh:

Year:  2018        PMID: 28915122     DOI: 10.1515/jpm-2017-0187

Source DB:  PubMed          Journal:  J Perinat Med        ISSN: 0300-5577            Impact factor:   1.901


  4 in total

1.  Genotype and phenotype variability in Sjögren-Larsson syndrome.

Authors:  Maximilian Weustenfeld; Reiner Eidelpes; Matthias Schmuth; William B Rizzo; Johannes Zschocke; Markus A Keller
Journal:  Hum Mutat       Date:  2018-11-26       Impact factor: 4.878

Review 2.  Sjogren-Larsson Syndrome: Mechanisms and Management.

Authors:  Parayil Sankaran Bindu
Journal:  Appl Clin Genet       Date:  2020-01-07

Review 3.  Variations in the Human Serum Albumin Gene: Molecular and Functional Aspects.

Authors:  Gianluca Caridi; Francesca Lugani; Andrea Angeletti; Monica Campagnoli; Monica Galliano; Lorenzo Minchiotti
Journal:  Int J Mol Sci       Date:  2022-01-21       Impact factor: 5.923

Review 4.  Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia.

Authors:  Lorenzo Minchiotti; Gianluca Caridi; Monica Campagnoli; Francesca Lugani; Monica Galliano; Ulrich Kragh-Hansen
Journal:  Front Genet       Date:  2019-04-17       Impact factor: 4.599

  4 in total

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