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The oro-dental phenotype in Prader–Willi syndrome: a survey of 15 patients

✍ Scribed by ISABELLE BAILLEUL-FORESTIER; VERONIEK VERHAEGHE; JEAN-PIERRE FRYNS; FRANS VINCKIER; DOMINIQUE DECLERCK; ANNICK VOGELS

Book ID
108829331
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
148 KB
Volume
0
Category
Article
ISSN
0960-7439

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Comparison of phenotype between patients
Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15
✍ Cassidy, S. B.; Forsythe, M.; Heeger, S.; Nicholls, R. D.; Schork, N.; Benn, P.; 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 241 KB 👁 2 views

Prader-Willi syndrome (PWS) is a complex multiple anomaly syndrome that has been shown to result from deficient expression of paternal chromosome 15(q11-q13). In most cases, it is caused either by deletion of this region in the paternally inherited chromosome 15 or by maternal uniparental disomy (UP