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1 OMIM reference -
1 associated gene
13 signs/symptoms
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
1 OMIM reference -
4 associated genes
No signs/symptoms info
Hereditary neuropathy with liability to pressure palsies
Dejerine-Sottas syndrome

PMP22 EGR2
MPZ
PMP22
PRX


COMMON
GENES
PMP22


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PMP22
(0.94)
MPZ



Citations in the biomedical literature:


Hereditary neuropathy with liability to pressure palsies
PMP22
Dejerine-Sottas syndrome
EGR2 MPZ PRX



Hereditary neuropathy with liability to pressure palsies
Dejerine-Sottas syndrome

Synonym(s):
- Current pressure-sensitive neuropathy
- HNPP
- Heterozygous microdeletion 17p11.2p12
- Potato-grubbing palsy
- Tomaculous neuropathy
- Tulip-bulb digger's palsy

Synonym(s):
- Charcot-Marie-Tooth disease type 3
- HMSN 3
- Hereditary motor and sensory neuropathy type 3
- Hypertrophic neuropathy of infancy

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: 1-9 / 100 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: -
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C538392

Hereditary neuropathy with liability to pressure palsies

Very frequent
- Autosomal dominant inheritance
- Insterstitial / subtelomeric microdeletion / deletion
- Nerve conduction abnormality
- Peripheral neuropathy

Frequent
- Motor deficit / trouble
- Paresthesia / dysesthesia / hypoesthesia / anesthesia / numbness
- Scoliosis

Occasional
- Abnormal cry / voice / phonation disorder / nasal speech
- Areflexia / hyporeflexia
- Cranial nerves palsy
- Flat palm
- Pes cavus
- Respiratory distress / dyspnea / respiratory failure / lung volume reduction


Dejerine-Sottas syndrome

(no data available)