Literature DB >> 33614549

Endocrine Diseases of Newborn: Epidemiology, Pathogenesis, Therapeutic Options, and Outcome "Current Insights Into Disorders of Calcium and Phosphate in the Newborn".

Tashunka Taylor-Miller1, Jeremy Allgrove1.   

Abstract

The physiology and regulation of bone minerals in the fetus and the newborn is significantly different from children and adults. The bone minerals calcium, phosphate and magnesium are all maintained at higher concentrations in utero to achieve adequate bone accretion. This is an integral component of normal fetal development which facilitates safe neonatal transition to post-natal life. When deciphering the cause of bone mineral disorders in newborns, the potential differential diagnosis list is broad and complex, including several extremely rare conditions. Also, significant discoveries including new embryological molecular genetic transcription factors, the role of active placental mineral transport, and hormone regulation factors have changed the understanding of calcium and phosphate homeostasis in the fetus and the newborn. This article will guide clinicians through an updated review of calcium and phosphate physiology, then review specific conditions pertinent to successful neonatal care. Furthermore, with the advancement of increasingly rapid molecular genetic testing, genomics will continue to play a greater role in this area of fetal diagnostics and prognostication.
Copyright © 2021 Taylor-Miller and Allgrove.

Entities:  

Keywords:  PTH; calcium; fibroblast growth factor 23; genetics; magnesium; phosphate; vitamin D

Year:  2021        PMID: 33614549      PMCID: PMC7892781          DOI: 10.3389/fped.2021.600490

Source DB:  PubMed          Journal:  Front Pediatr        ISSN: 2296-2360            Impact factor:   3.418


  2 in total

Review 1.  Vitamin D Metabolites: Analytical Challenges and Clinical Relevance.

Authors:  N Alonso; S Zelzer; G Eibinger; M Herrmann
Journal:  Calcif Tissue Int       Date:  2022-03-03       Impact factor: 4.000

2.  Case Report: Novel TRPM6 Mutations Cause Hereditary Hypomagnesemia With Secondary Hypocalcemia in a Chinese Family and a Literature Review.

Authors:  Yiran Han; Yajuan Zhao; Hua Wang; Liang Huo
Journal:  Front Pediatr       Date:  2022-07-12       Impact factor: 3.569

  2 in total

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