Autism spectrum disorder-epilepsy-arthrogryposis syndrome

Orpha code: 370943OMIM code: 615553

Definition

A form of congenital disorders of N-linked glycosylation characterized by distal arthrogryposis (mild flexion contractures of the fingers, deviation of the distal phalanges, swan-neck deformity), retromicrognathia, general muscle hypotonia, delayed psychomotor development, autism spectrum disorder (speech delay, abnormal use of speech, difficulties in initiating, understanding and maintaining social interaction, limited non-verbal communication and repetitive behavior), seizures, microcephaly and mild to moderate intellectual disability that becomes apparent with age.

Disease data
Classification

Disease

Synonyms
SLC35A3-CDG
SLC35A3-CDG
ORPHA code
370943
OMIM code
615553
ICD10 code
Q87.8
ICD11 code
-

No additional description.

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