Acta Scientific Paediatrics (ISSN: 2581-883X)

Short Communication Volume 3 Issue 4

Prader-Labhart-Willi Syndrome

Volodymyr S Andrukh*

Children's Hospital, Dolyna, Ukraine

*Corresponding Author: Volodymyr S Andrukh, Children's Hospital, Dolyna, Ukraine.

Received: February 24, 2020; Published: March 04, 2020

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  We present a clinical pattern of Prader-Labhart-Willi syndrome in a 16-month-old boy. The syndrome is characterized by the development of severe obesity and delayed psychomotor and sexual development as well as a determined dysfunction of the РWS-АS site in the 15th pair of chromosomes of male origin. The peculiarity of the case is apnea manifestations, which are likely to lead to fatal outcome.

Keywords: Prader-Labhart-Willi; Syndrome; Children

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References

  1. A Popescu. “Pediatric Syndromes”. Bucharest Medical publishing house (1977): 302-303.
  2. SV Yarygina., et al. “Relevance and Possibility of Early Diagnostics of Prader-Willi Syndrome”. Pediatrics (2006): 118-119.
  3. Yames H. “Hutchison Practical paediatric problem”. London (1999): 224-225.
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Citation

Citation: Volodymyr S Andrukh. “Prader-Labhart-Willi Syndrome”. Acta Scientific Paediatrics 3.4 (2020): 22-23.



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