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Abstract
Citation: Ann Clin Case Rep. 2024;9(1):2569.DOI: 10.25107/2474-1655.2569
Management of Newborn with Parder-Willi Syndrome: A Case Report
Shally C*
Florence Nightingale College of Nursing, Guru Tegh Bahadur Hospital, India
*Correspondance to: Shally Chaudhary
PDF Full Text Case Report | Open Access
Abstract:
A case of Parder-Willi syndrome is described in a 2.5-year-old boy. He is positive with hypotonia and hyperphagia and failure to thrive with feeding problems in the neonatal period. Clinically he has dysmorphic features with widened nasal bridge, short stature, short hands and feet. The diagnosis was confirmed by gene mapping and DNA analysis. Early diagnosis was important for management of clinical signs, for parental counselling and for further investigations for stimulating the condition
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Cite the Article:
Shally C. Management of Newborn with Parder-Willi Syndrome: A Case Report. Ann Clin Case Rep. 2024; 9: 2569..
Journal Basic Info
- Impact Factor: 5.253*
- H-Index: 6
- ISSN: 2474-1655
- DOI: 10.25107/2474-1655
- PubMed NLM ID: 101702800
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