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1 OMIM reference -
1 associated gene
27 signs/symptoms
COMMON GENES: 1
COMMON SIGNS: 4
1 OMIM reference -
1 associated gene
12 signs/symptoms
Autosomal dominant Larsen syndrome
Spondylocarpotarsal synostosis

FLNB FLNB


COMMON
GENES
FLNB



Citations in the biomedical literature:


Autosomal dominant Larsen syndrome
FLNB
Spondylocarpotarsal synostosis



Autosomal dominant Larsen syndrome
Spondylocarpotarsal synostosis

Synonym(s):
(no synonyms)

Synonym(s):
- Synspondylism

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare maxillo-facial surgical disease
- Rare otorhinolaryngologic 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 / 1 000 000
Average age onset: neonatal/infancy
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: normal
Type of inheritance: autosomal recessive

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


COMMON
SIGNS
- Autosomal recessive inheritance
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Conductive deafness / hearing loss
- Vertebral segmentation anomaly / hemivertebrae


Autosomal dominant Larsen syndrome
Spondylocarpotarsal synostosis

Very frequent
- Absent / small fingernails / anonychia of hands
- Autosomal dominant inheritance
- Broad / bifid thumb
- Depressed nasal bridge
- Depressed premaxillary region / midface
- Flat face
- Frontal bossing / prominent forehead
- Hyperextensible joints / articular hyperlaxity
- Hypertelorism
- Joint dislocation / subluxation
- Long hand / arachnodactyly
- Short hand / brachydactyly

Frequent
- Wrist / carpal anomalies

Occasional
- Craniostenosis / craniosynostosis / sutural synostosis
- Epiphyseal anomaly
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Laryngomalacia
- Respiratory distress / dyspnea / respiratory failure / lung volume reduction
- Scoliosis
- Short stature / dwarfism / nanism
- Structural anomalies of the cardio-circulatory system
- Syndactyly of fingers / interdigital palm
- Undescended / ectopic testes / cryptorchidia / unfixed testes


Very frequent
- Abnormal vertebral size / shape
- Carpal bones fusion / synostosis
- Lordosis
- Restricted joint mobility / joint stiffness / ankylosis
- Short rib cage / thorax

Occasional
- Pectus excavatum
- Polycystic kidneys
- Sensorineural deafness / hearing loss