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1 OMIM reference -
1 associated gene
12 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
MASA syndrome
Congenital lethal myopathy, Compton-North type

L1CAM CNTN1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
L1CAM
(0.52)
CNTN1



Citations in the biomedical literature:


MASA syndrome
L1CAM
Congenital lethal myopathy, Compton-North type
CNTN1



MASA syndrome
Congenital lethal myopathy, Compton-North type

Synonym(s):
- Intellectual defici-aphasia-shuffling gait-adducted thumbs syndrome

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: no data available
Type of inheritance: x-linked recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
1 MeSH reference: C536029
External references:
1 OMIM reference -
No MeSH references

MASA syndrome

Very frequent
- Abnormal gait
- Clasp thumb / thumb adduction / distal thumb phalangeal bone deviated / large
- Hemiplegia / diplegia / hemiparesia / limb palsy
- Hypereflexia
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Short stature / dwarfism / nanism
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia
- X-linked recessive inheritance

Frequent
- Camptodactyly of fingers
- Clinodactyly of fifth finger

Occasional
- Corpus callosum / septum pellucidum total / partial agenesis
- Dilated cerebral ventricles without hydrocephaly


Congenital lethal myopathy, Compton-North type

(no data available)