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2 OMIM references -
2 associated genes
14 signs/symptoms
COMMON GENES: 1
1 OMIM reference -
1 associated gene
4 signs/symptoms
Isolated cloverleaf skull syndrome
Camptodactyly - tall stature - scoliosis - hearing loss

ERF FGFR3
FGFR3


COMMON
GENES
FGFR3



Citations in the biomedical literature:


Isolated cloverleaf skull syndrome
ERF FGFR3
Camptodactyly - tall stature - scoliosis - hearing loss



Isolated cloverleaf skull syndrome
Camptodactyly - tall stature - scoliosis - hearing loss

Synonym(s):
- Kleeblattschaedel syndrome

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: unknown
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant

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

Isolated cloverleaf skull syndrome
Camptodactyly - tall stature - scoliosis - hearing loss

Very frequent
- Autosomal dominant inheritance
- Beaked nose
- Depressed premaxillary region / midface
- High forehead
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Low set ears / posteriorly rotated ears
- Mid-facial hypoplasia / short / small midface
- Proptosis / exophthalmos
- Stillbirth / neonatal death

Frequent
- Abnormal vertebral size / shape
- Craniostenosis / craniosynostosis / sutural synostosis
- Dysostosis / chondrodysplasia / osteodysplasia / osteochondrosis / skeletal dysplasia
- Restricted joint mobility / joint stiffness / ankylosis
- Syndactyly of fingers / interdigital palm



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