Outline of New Born Baby checking of Neurological Illnesses | OMICS International | Abstract

The Neurologist: Clinical & Therapeutics Journal
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Outline of New Born Baby checking of Neurological Illnesses

Bodensteiner JB*
Department of Pediatric Neurology, Barrow Neurological Institute, St. Joseph's Children's Health Center, NY, U.S.A
*Corresponding Author: Bodensteiner JB, Department of Pediatric Neurology, Barrow Neurological Institute, St. Joseph's Children's Health Center, NY, U.S.A, Email: [email protected]

Received Date: Aug 12, 2022 / Published Date: Sep 12, 2022

Citation: Bodensteiner JB (2022) Outline of New Born Baby Checking of Neurological Illnesses. Neurol Clin Therapeut J 6: 124.DOI: 10.4172/nctj.1000124

Copyright: © 2022 Bodensteiner JB. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.



More than 400 different disorders fall under the umbrella of neuromuscular diseases, which are diverse in their phenotypic range. Due to their rarity and complexity, neuromuscular illnesses are frequently only discovered after a very long period of time, at which point irreparable muscle loss may reduce the effectiveness of treatments, when any are available. Neonatal screening may offer an answer for early detection and therapy in this situation. PRISMA standards were followed to perform a systematic evaluation of the literature in PubMed up to May 1, 2021, which included conditions with a clear involvement of the peripheral nervous system and classic neuromuscular illnesses (including central nervous system disease with severe neuropathy). We identified seven disorders for which newborn screening data were available: Krabbe disease, X-linked adrenoleukodystrophy, Pompe disease, Duchenne muscular dystrophy, spinal muscular atrophy, Myotonic dystrophy type, Krabbe disease, X-linked adrenoleuko- dystrophy, Pompe disease and metachromatic leukodystrophy. Changing from a biochemical to a genetic-based approach will require a global technical shift in newborn screening for neuromuscular diseases. In order for innovative medicines to be as effective as possible, the rapid development of therapy also necessitates the ability to quickly adjust the list of ailments treated.

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