CareLit · DOI-Nachweis · Ultraschall in der Medizin - European Journal of Ultrasound
Sonographic Variety in the detection of Noonan Syndrome – case report -
DOI 10.1055/s-0033-1354992
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Autor:innenA Fiedler, E Schleußner, D Schlembach
ZeitschriftUltraschall in der Medizin - European Journal of Ultrasound
Ausgabe10/2013
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Purpose: Noonan-Syndrom is an autosomal-dominant inherited chromosomal disorder which is mostly located in PTPN11-Gen, in KRAS-Gen, in SOS1-Gen and in RAF1-Gen. But most of the cases develop sporadically. The prevalence of the Noonan-Syndrome is 1:1000 – 2500 live births. The syndrome shows a wide variety of symptoms comprising heart failure, mental impairment, kryptorchism, Pterygium colli, microsomia, fazial dysmo…
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Zitierempfehlung
A Fiedler, E Schleußner, D Schlembach (2013) Sonographic Variety in the detection of Noonan Syndrome – case report -. Ultraschall in der Medizin - European Journal of Ultrasound (10). https://doi.org/10.1055/s-0033-1354992
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