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

Slides:



Advertisements
Similar presentations
Understanding patterns of inheritance
Advertisements

“Emery’s Elements of Medical genetics”
Cystic Fibrosis BY. MERCEDES.
By: Tyler Abel. Cardiovascular System  Enlarged Aorta (blood flow away from the heart)  Aorta tearing (separation of layers)  “Floppy” mitral valve.
Review of Otolaryngology related Pediatric Syndromes
Genetics of Stickler Syndrome
Alport Syndrome: Dealing with Hearing Loss and Advances in Technology
Darron Fors & Dr. Robert Seegmiller Brigham Young University
Sara Kline Period 6 3/25/10. What is Alport Syndrome?  Chromosomal disorder that damages tiny blood vessels in the kidneys - - these tiny blood vessels.
Osteogensis Imperfecta (OI) “Brittle bone disease”
Stickler Disease: Eye Michael Shapiro, MD Retina Consultants, LTD Chicago.
Autosomal recessive inheritance Risks to children where a parent is affected: the basics a tutorial to show how the genes segregate to give the typical.
Autosomal dominant inheritance Risks to children where both parents are affected: the basics a tutorial to show how the genes segregate to give the typical.
Craniofacial Disorders Julie A. Dunlap, MS, CCC-SLP SPHSC 543 Winter 2010.
27.3 Genetic Disorders Errors in the chromosome number
Ashley Osborne Quesha McClanahan Orchi Haghighi
Corrine Fillman, M.S., C.G.C. Connective Tissue Gene Tests (CTGT) 6580 Snowdrift Road, Suite 300 Allentown, PA
Stickler Syndrome: A Physician’s Overview. What do you hear? It could just be a Zebra and not a Horse!
STICKLER SYNDROME Corrine Fillman, M.S., C.G.C.
DR. ERNEST K. ADJEI FRCPath. DEPARTMENT OF PATHOLOGY SMS-KATH
Osteogenesis Imperfecta
Alport Syndrome Genetics and Diagnosis Martin Gregory, MD, PhD Professor of Medicine University of Utah Nothing to disclose.
O STEOGENESIS I MPERFECTA COL1A1 Katelynn Weber. O STEOGENESIS I MPERFECTA Characteristics 6/100,000 worldwide.
Osteogenesis imperfecta
Treacher Collins syndrome By R2 黃信豪. History (1)  This 4 y/o female is a victim of Treacher- Collins syndrome.  Multiple facial anormaly including hypoplastic.
Marfan Syndrome Also known as Arachnodactyly, MFS, & Marfan Syndrome Type 1 and Type 2 By: Kianna Thompson.
DNA STANDS FOR DEOXYRIBONUCLEIC ACID. THIS IS JUST A CHEMICAL WHICH IS PART OF THE HUMAN BODY. OFF THIS STRAND OF DNA, YOU WILL SEE A BASE. THIS IS WHERE.
Human Development: Prenatal-Toddler Problems in Prenatal Development.
Lesson 3 Family members often share a strong physical resemblance. What inherited characteristics are visible in this family? Heredity and Genetics.
Lesson 3 2/23/12 Heredity & Genetics Name a few traits that you inherited from a family member? What family member did you inherit the trait from?
By Mitch & Russell. How Does a person inherit it? Is it dominant or recessive?  This disease can be passed down from parent to child. It is autosomal.
Stickler Syndrome Study at the National Institutes of Health Nazli McDonnell M.D., Ph.D. Laboratory of Clinical Investigation National Institute on Aging.
Problems in Prenatal Development Mrs. Gudgeon. Losing a Baby When a baby is lost before 20 weeks of pregnancy it is called a miscarriage. If it occurs.
Blindness Stickler GB, Hughes W, Houchin P. Clinical features of hereditary progressive arthro-ophthalmopathy (Sticklersyndrome): a survey. Genet Med.
SPONDYLOEPIMETAPHYSEAL DYSPLASIA (STRUDWICK TYPE) Emily Walls & Zach Witherspoon.
Autosomal dominant inheritance: the basics a tutorial to show how the genes segregate to give the typical pedigree pattern Professor P Farndon, Clinical.
Group of inherited conditions with fragility of skin and mucous membranes (blisters and comes off easily) Abnormal protein connecting layers of skin.
Cockayne syndrome. Background: Cockayne syndrome: is a rare and devastating genetic disease. It is present in about 1/100,000 live births. Its inheritance.
Osteogenesis Imperfecta
Osteogenesis Imperfecta By Zachary G Brittle bone disease.
Ehlers-Danlos Syndromes Emily Chang AM report May 18, 2009.
Stickler’s Syndrome By Justin Leone Disease? Stickler’s Syndrome is a disorder, not a disease, that affects collagen throughout the body. Stickler’s.
Part I Amy L. McIntosh, MD Pediatric Orthopedic Surgeon Mayo Clinic Rochester, Minnesota.
Marfan Syndrome By: Oliver Bell. A mutation or a defect in the gene that makes Fibrillin- 1 (FBN1). Important part of connective tissue. Hereditary (Passed.
Chapter 4.2 – Problems in Prenatal Development
Genetic disorders can be due to any of the following factors: A. Monogenetic Disorders: Caused by a mutation in a single gene 1. Autosomal recessive alleles:
Autosomal recessive inheritance: the basics a tutorial to show how the genes segregate to give the typical pedigree pattern Professor P Farndon, Clinical.
Alström Syndrome.
A genetic disorder is an illness caused by one or more abnormalities in the genome, especially a condition that is present from birth (congenital). Most.
Marfan’s Syndrome By Emily Espinosa. History Bernard Marfan, a french pediatrician, described the disease that still bears his name at a meeting of the.
Usher Syndrome By Andy Beer. What is Usher Syndrome Usher Syndrome is a genetic disease on witch you lose the ability to hear and see. The major symptoms.
Table 1. Differential diagnosis (adapted from The Marfan Foundation)
Chromosomes and Inheritance Chapter 12 ( ).
Genetic Disorders  Common, with 2-4% of live-born babies having a significant congenital malformation and about 5% a genetic disorder.  30-50% of hospitalized.
Chapter 4.2: Problems in Prenatal Development
Usher syndrome By Andy Beer.
They all have “Unbreakable Spirits”
Hypermobility (and a little on inherited collagen disorders)
Budapest, Hungary - September 17-19, 2015
CONNECTIVE TISSUE DISORDERS
Cri du Chat Ilana Horton.
Class Notes #8: Genetic Disorders
Autosomal dominant inheritance: the basics
Birth Defects and Complications
Prenatal Development Problems.
Mutations that exist in the parents’ genes are inherited mutations.
Single gene conditions (also called monogenic conditions) are caused by abnormalities, or mutations, of a single gene. These conditions can be severe or.
The risk of siblings being affected depends on the mode of inheritance and the gender of the affected parent (in X-linked disease). The risk of siblings.
Presentation transcript:

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? What can we do to be in the best health possible?

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

Stickler Syndrome Eye Findings High Myopia Retinal tears and detachment Glaucoma Cataracts Snead MP, Eye 2011;

Joints Joint laxity Tall thin stature Degenerative Arthropathy Scoliosis Snead, MP; J Med Genet 36:

Craniofacial People with Stickler syndrome can resemble each other as well as their families U-shaped cleft palate Bifid uvula Pierre-Robin Sequence m Antunes RB, J Plastic Recon Aesth Surg 2012: 1029

Hearing Loss 80% Hypermobility Conductive Sensorineural Mixed Can worsen

Heart Mitral valve prolapse

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?

What causes Stickler syndrome? Collagen: the gel, the cushion, and the girders Compressible, Structural (crosslinking)

Where is collagen? Joints Bones Cornea and vitreous (eye) Skin Intestines Spinal disks Dentin (teeth) Muscle Usually made by fibroblasts

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

Collagen 9A1

What does COL9A1 do? Works with collagen 2 In hyaline cartilage (articular joints)

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?

Stickler Syndrome Family Matters

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

Chromosomes

Stickler Syndrome Inheritance Two types ▫Autosomal Dominant ▫Autosomal Recessive

Autosomal Dominant Inheritance Affected Parent to Affected Child

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

Autosomal Recessive Parents are carriers and not affected

Genes in Autosomal Recessive Stickler Syndrome COL9A1: Very Rare; Autosomal recessive ▫3 families COL9A2: Very Rare; Autosomal recessive ▫Two children in one family

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?

Genetic Counseling: Low Tech Autosomal dominant 50% risk with each pregnancy Autosomal recessive 25% risk with each pregnancy Level II ultrasound weeks: micrognathia For parents with all types of Stickler Syndrome ▫Amniocentesis or CVS  If familial mutation(s) known ▫Donor Egg ▫Donor Sperm ▫Adoption

Genetic Counseling: High Tech If we know the gene mutation in the family

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?

Unfortunately, this is not the answer

Ophthalmology Rheumatology Orthopedics Audiology Craniofacial Cardiology

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

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

Many Thanks To Our patients and families affected by Stickler syndrome Dr. Ruth Lieberfarb Dr. David Sweetser Dr. Joseph Thakuria