203 top medical experts on Pontocerebellar Hypoplasia Type 1 across 17 countries and 5 U.S. states, including 25 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Pontocerebellar Hypoplasia Type 1: A severe, genetic form of pontocerebellar hypoplasia (PCH) characterized by spinal cord anterior horn cell degeneration in addition to pontocerebellar hypoplasia. Clinically, patients manifest with a severe global development deficit that is evident early on from difficulties in feeding and swallowing
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Support Organizations
- Fetal Health Foundation
9786 S Holland Street
Littleton, CO 80127
Toll-free: 877-789-4673
Telephone: 303-932-0553
E-mail: info@fetalhealthfoundation.org
Website: http://www.fetalhealthfoundation.org/
- The Joshua Deeth Foundation
38 James Square
Second Floor
Room 2
Crieff, PH7 3EY Scotland
Telephone: 01764650949
Website: http://www.thejoshuadeethfoundation.co.uk/
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- Synonyms: Pontocerebellar Hypoplasia With Anterior Horn Cell Disease, Pontocerebellar Hypoplasia With Infantile Spinal Muscular Atrophy, Type 1a Pontocerebellar Hypoplasia
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