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1 OMIM reference -
1 associated gene
21 signs/symptoms
COMMON GENES: 1
COMMON SIGNS: 1
1 OMIM reference -
1 associated gene
4 signs/symptoms
Hypochondroplasia
Camptodactyly - tall stature - scoliosis - hearing loss

FGFR3 FGFR3


COMMON
GENES
FGFR3



Citations in the biomedical literature:


Hypochondroplasia
FGFR3
Camptodactyly - tall stature - scoliosis - hearing loss



Hypochondroplasia
Camptodactyly - tall stature - scoliosis - hearing loss

Synonym(s):
(no synonyms)

Synonym(s):
- CATSHL 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):
- Congenital malformations, deformations and chromosomal abnormalities -

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

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


COMMON
SIGNS
- Scoliosis


Hypochondroplasia
Camptodactyly - tall stature - scoliosis - hearing loss

Very frequent
- Abnormal vertebral size / shape
- Autosomal dominant inheritance
- Dysostosis / chondrodysplasia / osteodysplasia / osteochondrosis / skeletal dysplasia
- Short foot / brachydactyly of toes
- Short hand / brachydactyly
- Short limbs / micromelia / brachymelia
- Short stature / dwarfism / nanism

Frequent
- Elbow anomalies(excluding luxation)
- Femur anomaly / absence / agenesis / hypoplasia / bifurcation
- Genu varum
- Hyperextensible joints / articular hyperlaxity
- Metaphyseal anomaly
- Pelvis anomaly / Narrow / broad iliac wings / pubis abnormality

Occasional
- Apnea / sleep apnea
- Bowed diaphysis / diaphyses / long bones
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Lordosis
- Macrocephaly / macrocrania / megalocephaly / megacephaly
- Osteoarthritis
- Rachidian / spine canal stenosis


Very frequent
- Camptodactyly of fingers
- Hearing loss / hypoacusia / deafness
- Tall stature / gigantism / growth acceleration