Results 41 to 50 of about 15,656 (183)

Targeting the Gut Microbiome in Prader-Willi Syndrome [PDF]

, 2021
Overwhelming evidence demonstrates an important role of the gut microbiome in the development of a wide range of diseases, including obesity, metabolic disorders, and mental health symptoms.
Carles Lerin, Marta Ramon-Krauel, Mercedes Serrano, Antonio F. Martinez-Monseny, Montse Amat-Bou   +4 more
core   +1 more source

An Observational Study on Cephalometric Characteristics and Patterns Associated with the Prader–Willi Syndrome: A Structural Equation Modelling and Network Approach

Applied Sciences, 2021
Examining specific patterns of major cranio-facial alterations through cephalometric measurements in order to improve the Prader–Willi (PWS) syndrome diagnostic poses a major challenge of identifying interlinkages between numerous credentials.
Alin Viorel Istodor, Laura-Cristina Rusu, Gratiela Georgiana Noja, Alexandra Roi, Ciprian Roi, Emanuel Bratu, Georgiana Moise, Maria Puiu, Simona Sorina Farcas, Nicoleta Ioana Andreescu   +9 more
doaj   +1 more source

Supplementary Material for: Microdeletion 15q26.2qter and Microduplication 18q23 in a Patient with Prader-Willi-Like Syndrome: Clinical Findings [PDF]

, 2016
The small interstitial deletion in the long arm of chromosome 15 causing Prader-Willi/Angelman syndrome is well known, whereas cases that report terminal deletions in 15q in association with the Prader-Willi-like phenotype are very rare.
Dello Russo P. (3206583), Demori E. (3206586), Zoratti R. (3206577), Damante G. (3206571), Romagno D. (3206574), Sechi A. (3206589), Passon N. (3206568), Gnan C. (3206580)   +7 more
core   +1 more source

The transition from pediatric to adult care in individuals with Prader-Willi syndrome

Endocrine Connections, 2022
Prader–Willi syndrome (PWS), the most common form of syndromic obesity, is a complex neurodevelopmental genetic disorder including obesity with hyperphagia, endocrine and metabolic disorders and also psychiatric disorders.
Christine Poitou, Anthony Holland, Charlotte Höybye, Laura C G de Graaff, Sandrine Bottius, Berit Otterlei, Maithé Tauber   +6 more
doaj   +1 more source

The presentation, course and outcome of COVID-19 infection in people with Prader-Willi syndrome: unexpected findings from an international survey

Orphanet Journal of Rare Diseases, 2022
Background Prader-Willi syndrome (PWS), is a genetically determined neurodevelopmental disorder, associated with intellectual disabilities and a high incidence of obesity, diabetes mellitus, and respiratory disorders.
J. E. Whittington, A. J. Holland, D. J. Driscoll, N. Hodebeck-Stuntebeck, A. Hoctor   +4 more
doaj   +1 more source

Additional file 1: of The effects of Bifidobacterium animalis ssp. lactis B94 on gastrointestinal wellness in adults with Praderâ Willi syndrome: study protocol for a randomized controlled trial

, 2018
SPIRIT checklist. (PDF 169 kb)
Alyousif, Zainab, Miller, Jennifer, Sandoval, Mariana, MacPherson, Chad, Nagulesapillai, Varuni, Dahl, Wendy   +5 more
openaire   +1 more source

A case of adrenal myelolipoma complicated with Prader‐Willi syndrome

IJU Case Reports, 2023
Introduction Prader‐Willi syndrome is a congenital disorder that occurs in one in 10 000–30 000 children and is characterized by obesity, short stature, and intellectual disability.
Toru Inoue, Masahiro Todaka, Yuichi Nakazono, Yoko Fukata, Toshitaka Shin   +4 more
doaj   +1 more source

Additional file 2: of The effects of Bifidobacterium animalis ssp. lactis B94 on gastrointestinal wellness in adults with Praderâ Willi syndrome: study protocol for a randomized controlled trial

, 2018
World Health Organization Trial Registration Data Set. (PDF 98 kb)
Alyousif, Zainab, Miller, Jennifer, Sandoval, Mariana, MacPherson, Chad, Nagulesapillai, Varuni, Dahl, Wendy   +5 more
openaire   +1 more source

The importance of early recognition of Prader-Willi syndrome [PDF]

Due to its rare nature and subtle dysmorphisms, Prader-Willi syndrome can be challenging to recognize and diagnose in the neonatal period. Feeding difficulties and hypotonia ('floppy infant') are the most striking characteristics.
Burgers, Melanie, Klaassens, Merel, Janssen, Etienne J.M., Geelen, Joyce M., Kerkhof, Gerthe F., Sinnema, Margje   +5 more
core   +8 more sources

Baby food and bedtime: Evidence for opposite phenotypes from different genetic and epigenetic alterations in Prader-Willi and Angelman syndromes

SAGE Open Medicine, 2019
Prader–Willi and Angelman syndromes are often referred to as a sister pair of neurodevelopmental disorders, resulting from different genetic and epigenetic alterations to the same chromosomal region, 15q11-q13.
Iiro Ilmari Salminen, Bernard J Crespi, Mikael Mokkonen   +2 more
doaj   +1 more source