Reissland, Nadja and Makhmud, Akerke and Froggatt, Suzanne (2019) 'Comparing a foetus diagnosed with Prader-Willi-syndrome with non-affected foetuses during light and sound stimulation using 4D ultrasound.', Acta paediatrica., 108 (2). pp. 375-376.
Prader‐Willi syndrome (PWS) is a complex neuro‐genetic disorder with estimated prevalence varying from 1 in 10,000 to 1 in 30,000 with an equal number of males and females affected. A study of the incidence of PWS in France reported thirty‐eight infants were diagnosed at a median age of 18 days post birth. None of the cases were identified prenatally. The condition is complex with fetal PWS phenotype including fetal hypo‐mobility, polyhydramnios, intra‐uterine growth restriction, and immobile flexed extremities with clenched hands or fists, symptoms which are not exclusively pathognomonic to PWS.
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|Publisher Web site:||https://doi.org/10.1111/apa.14622|
|Publisher statement:||This is the accepted version of the following article: Reissland, Nadja, Makhmud, Akerke & Froggatt, Suzanne (2019). Comparing a fetus diagnosed with Prader-Willi-syndrome with non-affected foetuses during light and sound stimulation using 4D ultrasound. Acta Paediatrica 108(2): 375-376, which has been published in final form at https://doi.org/10.1111/apa.14622. This article may be used for non-commercial purposes in accordance With Wiley Terms and Conditions for self-archiving.|
|Date accepted:||26 October 2018|
|Date deposited:||27 November 2018|
|Date of first online publication:||26 October 2018|
|Date first made open access:||26 October 2019|
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