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Wilson-Turner syndrome
1 OMIM reference -
1 associated gene
38 signs/symptoms
PROTEIN INTERACTIONS: 2
COMMON SIGNS: 1
Congenital fiber-type disproportion myopathy
2 OMIM references -
7 associated genes
8 signs/symptoms
Wilson-Turner syndrome
Congenital fiber-type disproportion myopathy

HDAC8
(UniProt - OMIM)
 ACTA1
(UniProt - OMIM)
ITGA7
(UniProt - OMIM)
MYL2
(UniProt - OMIM)
PTPLA
(UniProt - OMIM)
SEPN1
(UniProt - OMIM)
TPM2
(UniProt - OMIM)
TPM3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HDAC8
HDAC8
(0.72)
(0.63)
TPM3
ACTA1


Citations in the biomedical literature:


Wilson-Turner syndrome
HDAC8
Congenital fiber-type disproportion myopathy
ACTA1 ITGA7 MYL2 PTPLA SEPN1 TPM2
TPM3



Wilson-Turner syndrome
Congenital fiber-type disproportion myopathy

Synonym(s):
- X-linked intellectual deficit - gynecomastia - obesity
Synonym(s):
- CFTDM
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: x-linked dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references
COMMON
SIGNS 		- Scoliosis

Wilson-Turner syndrome
Congenital fiber-type disproportion myopathy

Very frequent
- Generalized obesity

Frequent
- Gynecomastia / breast / mammary gland enlargement / hyperplasia
- Small / atrophic / hypoplastic testes / monorchism / microorchidism / anorchia
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia

Occasional
- Abnormal cry / voice / phonation disorder / nasal speech
- Abnormal gait
- Anodontia / oligodontia / hypodontia
- Arthritis / synovitis / synovial proliferation
- Ataxia / incoordination / trouble of the equilibrium
- Brachycephaly / flat occiput
- Coarse face
- Hirsutism / hypertrichosis / Increased body hair
- Hypotrichosis / atrichia / atrichiasis / scalp hairlessness
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Irregular length / shape of fingers
- Long / large ear
- Lymphedema
- Maternal hypertension / eclampsia / preeclampsia / gravidic toxemia
- Micropenis / small penis / agenesis
- Microstomia / little mouth
- Microtia / cryptomicrotia / anotia / external auditory canal / pinnae aplasia / hypoplasia
- Pointed chin
- Preauricular / branchial tags / appendages
- Prognathism / prognathia
- Protruding lips
- Round ear
- Seizures / epilepsy / absences / spasms / status epilepticus
- Small hand / acromicria
- Small / hypoplastic / adherent / absent ear lobe
- Spindle shaped fingers
- Striae
- Synophris / synophrys
- Tapered fingers
- Thick / bushy eyebrows
- Thick / wide ear lobe
- Umbilical hernia
- Undescended / ectopic testes / cryptorchidia / unfixed testes


Very frequent
- Abnormal muscle biopsy / muscle enzymes / CPK / LDH / aldolase / creatin phosphokinase
- Areflexia / hyporeflexia
- Autosomal recessive inheritance
- Hypotonia
- Myopathy

Frequent
- Pectus excavatum
- Repeat respiratory infections