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Premature newborn with severe central hypotonia and cryptorchidism


Authors: S. Čičová;  E. Oríšková;  A. Valachová;  P. Šimurka
Authors‘ workplace: Klinika pediatrie a neonatológie, Fakultná nemocnica Trenčín, Slovensko
Published in: Čes-slov Pediat 2019; 74 (5): 271-274.
Category: Case Report

Overview

Authors present a case report of preterm newborn with intrauterine growth retardation and cryptorchidism. Severe central hypotonia with pooor suck were persistant symptoms. We have suspicion to Prader-Willi syndrome, which was confirmed by special genetic tests.

Keywords:

hypotonic syndrome – newbord – Prader-Willi syndrome – Cryptorchidism


Sources

1. Deepak MK, et al. Quick Reference Guide to Pediatric Care. 2nd ed. USA: American Academy of Pediatrics, 2018: 892–898.

2. Lebl J, Al Taji E, a kol. Malý atlas dětskej endokrinologie. Praha: Galén, 2013: 26–27.

3. Scheimann A, Rohena L. Prader-Willi syndrome. http://emedicine.medscape.com/article/947954-overview/.

4. Butler GM. Prader Willi syndrome. http://rarediseases.org/rare-diseases/prader-willi-syndrome.

5. Košťálová Ľ. Liečba rastovým hormónom v detskom veku. Pediatr Praxi 2008; 9 (3): 181–186.

Labels
Neonatology Paediatrics General practitioner for children and adolescents
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