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

Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome.

American journal of medical genetics. Part A - 1 Mar 2015

Boot Erik, Butcher Nancy J, van Amelsvoort Thérèse A M J, Lang Anthony E, Marras Connie, Pondal Margarita, Andrade Danielle M, Fung Wai Lun Alan, Bassett Anne S

Abstract excerpt

Movement abnormalities are frequently reported in children with 22q11.2 deletion syndrome (22q11.2DS), but knowledge in this area is scarce in the increasing adult population. We report on five individuals illustrative of movement disorders and other motor abnormalities in adults with 22q11.2DS. In addition to an increased susceptibility to neuropsychiatric disorders, seizures, and early-onset Parkinson disease,...

Read the complete abstract on PubMed

Topics

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

Share to Young Adult
Share to Tremor

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Clozapine

Share to Diagnosis, Differential

Share to DiGeorge Syndrome

Share to Movement Disorders

Share to Myoclonus

Share to Parkinsonian Disorders

Source

Open in PubMed Open full text

Identifiers

PMID: 25684639
DOI: 10.1002/ajmg.a.36928
PMCID: PMC4459830

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

Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome.PMID 25684639Read ↗

Dissecting the Phenotypic Spectrum and Complexity of Movement Disorders in 22q11.2 Deletion Syndrome.Semantic proximity Read ↗

Neurological manifestation of 22q11.2 deletion syndromeSemantic proximity Read ↗

Phenotypic and Genetic Complexity in Pediatric Movement DisordersSemantic proximity Read ↗

Pediatric movement disorders.Semantic proximity Read ↗

Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion SyndromeSemantic proximity Read ↗

16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.Semantic proximity Read ↗

Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications.Semantic proximity Read ↗

The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan.Semantic proximity Read ↗

Diagnostic approach to paediatric movement disorders: a clinical practice guide.Semantic proximity Read ↗

Parkinson's disease associated with 22q11.2 deletion: Clinical characteristics and response to treatment.Semantic proximity Read ↗

Behavioral and Psychiatric Phenotypes in 22q11.2 Deletion SyndromeSemantic proximity Read ↗

A Comprehensive Review of Secondary Movement DisordersSemantic proximity Read ↗

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