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Champ1-related intellectual disability-facial dysmorphism-behavioural abnormalities syndrome

Engelsk navn: CHAMP1-related intellectual disability-facial dysmorphism-behavioral abnormalities syndrome
ORPHA-kode 692193
Klassifikasjon

Klassifisering

Orphanet sitt klassifiseringssystem har tre nivåer for å organisere de sjeldne diagnosene: Group (gruppe), disorder (diagnose) og subtype (undertype).
Disorder

Definisjon

A rare malformation syndrome characterized by global developmental delay with intellectual disability, speech delay, hypotonia, neurobehavioral symptoms including autism spectrum disorder, repetitive behaviors, attention deficit hyperactivity disorder, and sleep abnormalities. Dysmorphic facial features may include microcephaly (or sometimes macrocephaly), a round face, a flat head with a shortened forehead, hypertelorism, upslanted palpebral fissures, bulbous nose, wide nasal bridge, short philtrum, tented upper lip, and dental abnormalities (most commonly retained primary teeth). Additional clinical features can include recurrent infections, cyclic vomiting syndrome, seizures, and nonspecific congenital malformations.
Informasjonen om denne diagnosen er hentet fra Orpha.net.

Mer om diagnosen

Denne diagnosen har per i dag ikke et tilbud i en kompetanseenhet, men det er registrert tilfeller av diagnosen i Norge. Kontakt

Ekstern informasjon

Deler av informasjonen over er hentet fra ORPHAdata med lisens: Commons Attribution 4.0 International (CC BY 4.0)