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Metaphyseal chondrodysplasia, Jansen type

1 OMIM reference -
1 associated gene
20 signs/symptoms

COMMON GENES: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Metaphyseal chondrodysplasia, Jansen type

Eiken syndrome

PTH1R

(UniProt - OMIM)

(UniProt - OMIM)


COMMON GENES	PTH1R

Citations in the biomedical literature:

Metaphyseal chondrodysplasia, Jansen type		Eiken syndrome

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - 1 MeSH reference: C537564		External references: 1 OMIM reference - No MeSH references

Metaphyseal chondrodysplasia, Jansen type
	Very frequent - Dense / thickened skull / calvarium / cranial / facial hyperostosis - Frontal bossing / prominent forehead - Hypertelorism - Metaphyseal anomaly - Micrognathia / retrognathia / micrognathism / retrognathism - Prominent supraorbital ridge - Proptosis / exophthalmos - Restricted joint mobility / joint stiffness / ankylosis - Short limbs / micromelia / brachymelia - Short stature / dwarfism / nanism Frequent - Clinodactyly of fifth finger - Enlarged diaphysis / diaphyses - Hypercalcemia - Hypoparathyroidy - Hypoplastic mandibula / partial absence of the mandibula - Narrow rib cage / thorax - Osteosclerosis / osteopetrosis / bone condensation - Phosphocalcic metabolism anomalies - Short hand / brachydactyly Occasional - Sensorineural deafness / hearing loss
Eiken syndrome
(no data available)