Journal Basic Info

  • Impact Factor: 1.809**
  • H-Index: 6
  • ISSN: 2474-1655
  • DOI: 10.25107/2474-1655
**Impact Factor calculated based on Google Scholar Citations. Please contact us for any more details.

Major Scope

  •  Diabetology
  •  Renal Disease
  •  Signs and Symptoms-Clinical Findings
  •  Pediatrics
  •  Urology Cases
  •  Ophthalmology
  •  Psychiatry and Mental Health
  •  Pathology


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


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


Cite the Article:

Shally C. Management of Newborn with Parder-Willi Syndrome: A Case Report. Ann Clin Case Rep. 2024; 9: 2569..

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