Das prader-Labhart-Willi-syndrom im säuglingsalter

Translated title of the contribution: Prader-Labhart-Willi syndrome in infants

Heinrike Schmeling, G. Gillessen-Kaesbach, U. Schulte-Mattler, S. Burdach, G. Horneff*

*Corresponding author for this work
1 Citation (Scopus)


We report an infant with severe hypotonia, feeding problems and failure to thrive in the neonatal period, followed by developmental delay. In addition, pale skin, eyelid and pedal edema, cryptorchidism and micrognathia were present. The tentative diagnosis of Prader-Labhart-Willi syndrome was made and confirmed by specific molecular testing at the age of 5 months. The Prader-Labhart-Willi syndrome is usually diagnosed in older infants when the main clinical features such as obesity, short stature, hypogonadism and developmental delay become obvious, in most of the patients typical clinical features are present already in the neonatal period. In conclusion, in neonates and young infants presenting with hypotonia and feeding problems, the Prader-Labhart-Willi syndrome should be considered.

Translated title of the contributionPrader-Labhart-Willi syndrome in infants
Original languageGerman
JournalKlinische Padiatrie
Issue number2
Pages (from-to)51-53
Number of pages3
Publication statusPublished - 2002

Research Areas and Centers

  • Research Area: Medical Genetics


Dive into the research topics of 'Prader-Labhart-Willi syndrome in infants'. Together they form a unique fingerprint.

Cite this