Stickler syndrome, type 5
- Synonyms
- COL9A2-Related Stickler Syndrome
Summary
Excerpted from the GeneReview:Stickler syndrome is a connective tissue disorder that can include ocular findings of myopia, cataract, and retinal detachment; hearing loss that is both conductive and sensorineural; midfacial underdevelopment and cleft palate (either alone or as part of the Pierre Robin sequence); and early-onset degenerative joint disease. Variable phenotypic expression of Stickler syndrome occurs both within and among families; interfamilial variability is in part explained by locus and allelic heterogeneity.
- Full text of GeneReview (by section):
- Summary
- Diagnosis
- Clinical Characteristics
- Genetically Related (Allelic) Disorders
- Differential Diagnosis
- Management
- Genetic Counseling
- Resources
- Molecular Genetics
- Chapter Notes
- References
- Authors:
- Geert Mortier
- view full author information
Available tests
65 tests are in the database for this condition.
Check Related conditions for additional relevant tests.
Clinical tests (65 available)
Clinical features
Help- Abnormality of head or neck
- Isolated Pierre-Robin syndrome
Isolated Pierre-Robin syndrome
- MedGen UID: 19310
- Concept ID: C0031900
- Finding: Congenital Abnormality
Abnormality of head or neck
- Midface retrusion
Midface retrusion
- MedGen UID: 339938
- Concept ID: C1853242
- Finding: Anatomical Abnormality
Abnormality of head or neck
- Short chin
Short chin
- MedGen UID: 784514
- Concept ID: C3697248
- Finding: Finding
Abnormality of head or neck
- Isolated Pierre-Robin syndrome
- Abnormality of the eye
- Cataract
Cataract
- MedGen UID: 39462
- Concept ID: C0086543
- Finding: Disease or Syndrome
Abnormality of the eye
- High myopia
High myopia
- MedGen UID: 78759
- Concept ID: C0271183
- Finding: Disease or Syndrome
Abnormality of the eye
- Retinal detachment
Retinal detachment
- MedGen UID: 19759
- Concept ID: C0035305
- Finding: Disease or Syndrome
Abnormality of the eye
- Vitreoretinopathy
Vitreoretinopathy
- MedGen UID: 87480
- Concept ID: C0344290
- Finding: Disease or Syndrome
Abnormality of the eye
- Cataract
- Ear malformation
- Sensorineural hearing loss disorder
Sensorineural hearing loss disorder
- MedGen UID: 9164
- Concept ID: C0018784
- Finding: Disease or Syndrome
Ear malformation
- Sensorineural hearing loss disorder
- Growth abnormality
- Short stature
Short stature
- MedGen UID: 87607
- Concept ID: C0349588
- Finding: Finding
Growth abnormality
- Short stature
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