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Shprintzen-Goldberg syndrome
1 OMIM reference -
2 associated genes
55 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 3
Branchio-otic syndrome
3 OMIM references -
2 associated genes
18 signs/symptoms
Shprintzen-Goldberg syndrome
Branchio-otic syndrome

FBN1
(UniProt - OMIM)
 EYA1
(UniProt - OMIM)
SKI
(UniProt - OMIM)
 SIX1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SKI
(0.63)
SIX1


Citations in the biomedical literature:


Shprintzen-Goldberg syndrome
FBN1 SKI
Branchio-otic syndrome
EYA1 SIX1



Shprintzen-Goldberg syndrome
Branchio-otic syndrome

Synonym(s):
- Marfanoid craniosynostosis syndrome
- SGS
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare otorhinolaryngologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: no data available
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: C537328
External references:
3 OMIM references -
No MeSH references
COMMON
SIGNS 		- Autosomal dominant inheritance
- Conductive deafness / hearing loss
- Micrognathia / retrognathia / micrognathism / retrognathism

Shprintzen-Goldberg syndrome
Branchio-otic syndrome

Very frequent
- Dolichocephaly / scaphocephaly
- Downslanted palpebral fissures / anti-mongoloid slanting palpebral fissures
- Flat foot
- High vaulted / narrow palate
- Hypertelorism
- Hypotonia
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Long hand / arachnodactyly
- Low set ears / posteriorly rotated ears
- Marfanoid morphotype
- Proptosis / exophthalmos
- Telecanthus / canthal dystopy

Frequent
- Aortic valve anomaly / incompetence / insufficiency / regurgitation / bicuspid
- Camptodactyly of some fingers
- Communicating hydrocephaly
- Craniostenosis / craniosynostosis / sutural synostosis
- Flexion deformity of toes (excluding big toe) / hammer toe / camptodactyly of toes
- Frontal bossing / prominent forehead
- High forehead
- Hyperextensible joints / articular hyperlaxity
- Hypoplastic maxillary bones / zygomatic bones / maxillary hypoplasia
- Inguinal / inguinoscrotal / crural hernia
- Mitral valve prolapse / incompetence / insufficiency / regurgitation / ring anomaly
- Pectus carinatum
- Pectus excavatum
- Ptosis
- Scoliosis
- Strabismus / squint
- Talipes-varus / metatarsal varus
- Umbilical hernia

Occasional
- Abnormal vertebral size / shape
- Absent / hypotonic / flaccid abdominal wall muscles
- Anteverted nares / nostrils
- Apnea / sleep apnea
- Arnold-Chiari anomaly
- Bowed diaphysis / diaphyses / long bones
- Dilated cerebral ventricles without hydrocephaly
- Elbow dislocation
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Gastroesophageal reflux / pyrosis / esophagitis / hiatal hernia / gastroparesia
- Genu valgum
- Hyperelastic skin / cutaneous hyperlaxity
- Large fontanelle / delayed fontanelle closure
- Metaphyseal anomaly
- Microcephaly
- Myopia
- Narrow rib cage / thorax
- Osteoporosis / osteopenia / demineralisation / osteomalacia / rickets
- Prominent / bat ears
- Restricted joint mobility / joint stiffness / ankylosis
- Rib number anomalies
- Undescended / ectopic testes / cryptorchidia / unfixed testes


Very frequent
- Branchial / posterior auricular / preauricular / cheek cysts / fistulae
- Dermoid sinus / dimple / pit (excluding sacral)
- Hearing loss / hypoacusia / deafness

Frequent
- Branchial fistulae of the neck
- External auditory canal atresia / stenosis / agenesis
- External ear anomalies
- Sensorineural deafness / hearing loss
- Structural anomalies of inner ear / cochlea / vestible / semicircular canals
- Structural anomalies of middle ear / ossicles / tympanic cavity

Occasional
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Defect / anomaly of lacrimal system
- Facial palsy
- Facial structural asymmetry / facial hemiatrophy / facial hemihypertrophy
- Lip pits / fistulae
- Preauricular / branchial tags / appendages