Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome-Reference-Cited by-同舟云学术

Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome

Published:2018-08-29 Issue:1 Volume:18 Page:
ISSN:1471-2431
Container-title:BMC Pediatrics
language:en
Short-container-title:BMC Pediatr

Author:

Ghedira Nehla,Lagarde Arnaud,Ben Ameur Karim,Elouej Sahar,Sakka Rania,Kerkeni Emna,Chioukh Fatma-Zohra,Olschwang Sylviane,Desvignes Jean-Pierre,Abdelhak Sonia,Delague Valerie,Lévy Nicolas,Monastiri Kamel,De Sandre-Giovannoli Annachiara

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1186/s12887-018-1259-8.pdf

Reference46 articles.

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2. Turner AM. Noonan syndrome. J Paediatr Child Health. 2014;50:E14–E20.

3. Romano AA, Allanson JE, Dahlgren J, Gelb BD, Hall B, Pierpont ME, et al. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010;126:746–59.

4. Van der Burgt I, Berends E, Lommen E, Van Beersum S, Hamel B, Mariman E. Clinical and molecular studies in a large Dutch family with Noonan syndrome. Am J Med Genet. 1994;53:187–91.

5. Zenker M. Genetic and pathogenetic aspects of Noonan syndrome and related disorders. Horm Res. 2009;72:57–63.

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