Article

Perinatal features of Prader-Willi syndrome: a Chinese cohort

2019-03-05

Abstract excerpt

<h4>Background</h4> Prader-Willi syndrome (PWS) is a rare complex genetic disorder caused by an absence of expression of imprinted genes on the paternally derived chromosome 15q11-q13 region. This study aimed to characterize the perinatal features in a cohort of Chinese individuals with PWS. <h4>Methods</h4> We analyzed anonymous data of 134 patients from the PWS Registry in China. Perinatal and neonatal present...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 90c3681c-cdfe-50d3-8967-7ed8f3c6ceb1
DOI: 10.1101/568451

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Perinatal features of Prader-Willi syndrome: a Chinese cohortDOI 10.1101/568451Read

Multicentre study of maternal and neonatal outcomes in individuals with Prader-Willi syndromeSemantic proximity Read

Clinical and genetic features of Prader-Willi syndrome in China.Semantic proximity Read

Possibilities and Limitations of Prenatal Diagnosis of Rare Imprinting Syndromes: Prader–Willi SyndromeSemantic proximity Read

Prader-Willi syndrome.Semantic proximity Read

Prader-Willi-like phenotypes: a systematic review of their chromosomal abnormalities.Semantic proximity Read

Comparison of perinatal factors in deletion versus uniparental disomy in Prader-Willi syndrome.Semantic proximity Read

[Prader-Willi syndrome in 2015].Semantic proximity Read

Prader-Willi Syndrome - Clinical Genetics, Diagnosis and Treatment Approaches: An UpdateSemantic proximity Read

Prader-Willi syndrome in Taiwan.Semantic proximity Read

Genotype-phenotype characteristics of 57 patients with Prader-Willi syndrome: a single-center experience from Turkey.Semantic proximity Read

Early diagnosis and care is achieved but should be improved in infants with Prader-Willi syndrome.Semantic proximity Read

Prader-Willi Syndrome: Clinical Genetics and Diagnostic Aspects with Treatment Approaches.Semantic proximity Read