Autism spectrum disorder-epilepsy-arthrogryposis syndrome

Orpha code: 370943OMIM code: 615553

Definicja

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
Klasyfikacja

Disease

Synonimy
SLC35A3-CDG
SLC35A3-CDG
Kod ORPHA
370943
Kod OMIM
615553
Kod ICD10
Q87.8
Kod ICD11
-

No additional description.

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