Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Growth patterns of patients with 1p36 deletion syndrome.

Congenital anomalies - 1 May 2014

Sangu Noriko, Shimojima Keiko, Shimada Shino, Ando Tomohiro, Yamamoto Toshiyuki

Abstract excerpt

1p36 deletion syndrome is one of the most common subtelomeric deletion syndromes. Obesity is frequently observed in patients with this syndrome. Thus, it is important to evaluate the growth status of an individual patient. For this purpose, we accumulated recorded growth data from 44 patients with this syndrome and investigated the growth patterns of patients. Most of the patients showed weight parameters within...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Body Weight
Share to Chromosome Deletion
Share to Chromosome Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 1

Share to In Situ Hybridization, Fluorescence

Share to Obesity

Share to Prader-Willi Syndrome

Share to Weight Gain

Source

Identifiers

PMID: 24750553
DOI: 10.1111/cga.12029

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Growth patterns of patients with 1p36 deletion syndrome.PMID 24750553Read ↗

Mild developmental delay and obesity in two patients with mosaic 1p36 deletion syndrome.Semantic proximity Read ↗

Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype.Semantic proximity Read ↗

Delineating the phenotype of 1p36 deletion in adolescents and adults.Semantic proximity Read ↗

Anthropometric characteristics of newborns with Prader–Willi syndromeSemantic proximity Read ↗

Mini-Review: Monosomy 1p36 syndrome: reviewing the correlation between deletion sizes and phenotypes.Semantic proximity Read ↗

Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi SyndromeSemantic proximity Read ↗

Age- and gender-dependent obesity in individuals with 16p11.2 deletion.Semantic proximity Read ↗

Growth Trajectories in Genetic Subtypes of Prader-Willi Syndrome.Semantic proximity Read ↗

First-year growth in children with Noonan syndrome: Associated with feeding problems?Semantic proximity Read ↗

Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems.Semantic proximity Read ↗

Mowat-Wilson Syndrome: Growth ChartsSemantic proximity Read ↗

Normative growth charts for individuals with Costello syndrome.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.