Consensus recommendations on altered sensory functioning in Phelan-McDermid syndrome.

Walinga, Margreet; Jesse, Sarah; Alhambra, Norma; Van Buggenhout, Griet

Walinga, Margreet; Jesse, Sarah; Alhambra, Norma; Van Buggenhout, Griet.

Affiliation

Walinga M; University of Groningen, University Medical Center Groningen, Dept. Genetics, Groningen, the Netherlands. Electronic address: m.j.walinga@umcg.nl.
Jesse S; University of Ulm, Department of Neurology, Ulm, Germany.
Alhambra N; Phelan-McDermid Association, Spain.
Van Buggenhout G; Department of Human Genetics, University Hospital Leuven, Belgium.

Eur J Med Genet ; 66(5): 104726, 2023 May.

Article in En | MEDLINE | ID: mdl-36796507

Subject(s)

Autism Spectrum Disorder; Chromosome Disorders; Humans; Autism Spectrum Disorder/genetics; Consensus; Chromosome Disorders/genetics; Chromosome Disorders/diagnosis; Chromosome Deletion; Chromosomes, Human, Pair 22/genetics

Key words

Guideline; Pain; Phelan-McDermid syndrome; SHANK3; Sensory dysfunction; Sensory processing disorder

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosome Disorders / Autism Spectrum Disorder Type of study: Diagnostic_studies / Guideline Limits: Humans Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2023 Type: Article

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