Stickler Syndrome: A Family Story

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Stickler Syndrome: A Family Story Paula Goldenberg, MD, MSW, MSCE 18 th American Stickler Syndrome Conference Denver, Colorado July 12, 2014

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Stickler Syndrome: A Family Story. Paula Goldenberg, MD, MSW, MSCE 18 th American Stickler Syndrome Conference Denver, Colorado July 12, 2014. Stickler Syndrome Basics What causes Stickler Syndrome? How Stickler Syndrome is passed down in families? How can we modify our genetic risk? - PowerPoint PPT Presentation

Transcript of Stickler Syndrome: A Family Story

Page 1: Stickler Syndrome: A Family Story

Stickler Syndrome:A Family StoryPaula Goldenberg, MD, MSW, MSCE18th American Stickler Syndrome ConferenceDenver, ColoradoJuly 12, 2014

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•Stickler Syndrome Basics•What causes Stickler Syndrome?•How Stickler Syndrome is passed down in

families?•How can we modify our genetic risk?•What can we do to be in the best health

possible?

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Stickler Syndrome

•Common (1:7500-1:9000 births)•Hereditary arthro-ophthalmopathy•Hearing loss is common in people with

Stickler syndrome•Most common genetic association in

patients with Pierre Robin sequence•Can affect many individuals in a family

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Stickler SyndromeEye Findings

•High Myopia•Retinal tears and detachment•Glaucoma•Cataracts

Snead MP, Eye 2011;1389-1400

http://epharmapedia.com

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Joints

•Joint laxity•Tall thin stature•Degenerative Arthropathy•Scoliosis

Snead, MP; J Med Genet 36:353-359

http://www.qt.com.au

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Craniofacial

•People with Stickler syndrome can resemble each other as well as their families

•U-shaped cleft palate•Bifid uvula•Pierre-Robin Sequence

http://ginoyton.com

Antunes RB, J Plastic Recon Aesth Surg 2012: 1029

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Hearing Loss

•80%•Hypermobility•Conductive•Sensorineural•Mixed•Can worsen

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Heart

•Mitral valve prolapse

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•Stickler Syndrome Basics•What causes Stickler Syndrome?•How Stickler Syndrome is passed down in

families?•How can we modify our genetic risk?•What can we do to be in the best health

possible?

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What causes Stickler syndrome?

•Collagen: the gel, the cushion, and the girders

•Compressible, Structural (crosslinking)

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Where is collagen?

•Joints•Bones•Cornea and vitreous (eye)•Skin•Intestines•Spinal disks•Dentin (teeth)•Muscle•Usually made by fibroblasts

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Collagen: Many varieties!•Type I-Type XXVIII!•Each type has different properties and uses•1,000 identified disease-causing mutations•Different types of collagen mutations can

cause▫Brittle Bone Disease (osteogenesis imperfecta)▫Ehlers-Danlos Syndromes (many types)▫Alport Syndrome (kidney failure and hearing

loss)▫Stickler Syndrome▫And many, many others

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Collagen 9A1

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What does COL9A1 do?

•Works with collagen 2•In hyaline cartilage (articular joints)

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•Stickler Syndrome Basics•What causes Stickler Syndrome?•How Stickler Syndrome is passed down in

families?•How can we modify our genetic risk?•What can we do to be in the best health

possible?

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Stickler SyndromeFamily Matters

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Stickler Syndrome

•Majority of patients have a parent with Stickler syndrome

•If a patient is the first person with Stickler syndrome in the family we call this a de novo deletion

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Chromosomes

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Stickler Syndrome Inheritance

•Two types▫Autosomal Dominant▫Autosomal Recessive

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Autosomal Dominant InheritanceAffected Parent to Affected Child

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Genes in Autosomal Dominant Stickler Syndrome•COL2A1: 80-90% Autosomal Dominant

▫Membranous vitreous anomaly with mild hearing loss

•COL11A1: 10-20% Autosomal Dominant▫Beaded vitreous anomaly with significant

hearing loss•COL11A2: Rare Autosomal Dominant

▫“Non-ocular” Stickler Syndrome

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Autosomal RecessiveParents are carriers and not affected

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Genes in Autosomal Recessive Stickler Syndrome•COL9A1: Very Rare; Autosomal recessive

▫3 families•COL9A2: Very Rare; Autosomal recessive

▫Two children in one family

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•Stickler Syndrome Basics•What causes Stickler Syndrome?•How Stickler Syndrome is passed down in

families?•How can we modify our genetic risk?•What can we do to be in the best health

possible?

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Genetic Counseling: Low Tech• Autosomal dominant 50% risk with each

pregnancy• Autosomal recessive 25% risk with each

pregnancy• Level II ultrasound 18-20 weeks: micrognathia• For parents with all types of Stickler Syndrome

▫Amniocentesis or CVS If familial mutation(s) known

▫Donor Egg▫Donor Sperm▫Adoption

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Genetic Counseling: High Tech

•If we know the gene mutation in the family

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•Stickler Syndrome Basics•What causes Stickler Syndrome?•How Stickler Syndrome is passed down in

families?•How can we modify our genetic risk?•What can we do to be in the best

health possible?

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Unfortunately, this is not the answer

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Genetics Clinic

OphthalmologyRheumatologyOrthopedics

AudiologyCraniofacial

Cardiology

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Excellent Care: it takes a village!

• Ophthalmology• Orthopedics• Rheumatology• Audiology• Craniofacial Team (Clefts, Pierre Robin)• Oral Maxillofacial Specialists• Cardiology• Genetics

▫Genetic Testing▫Can be a quarterback for the team▫Surveillance

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The village continued…

•Physical Therapy•Occupational Therapy•Physical Medicine and Rehabilitation•Vision Therapy•Hearing Aid Specialist•Social Work•Stickler Involved People•Stickler Syndrome Support Group (UK)•Facebook networks

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Many Thanks To

•Our patients and families affected by Stickler syndrome

•Dr. Ruth Lieberfarb•Dr. David Sweetser•Dr. Joseph Thakuria

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