Stickler syndrome
From Wikipedia, the free encyclopedia
| ICD-10 | Q87.8 |
|---|---|
| ICD-9 | 756.0 |
Stickler syndrome (or David-Stickler syndrome or Stickler-Wagner syndrome) is a group of inherited connective tissue disorders affecting collagen. It was first studied and characterised by Dr. G.B. Stickler in 1965. Stickler syndrome is a subtype of collagenopathy, types II and XI. Stickler syndrome is characterized by a distinctive facial appearance, eye abnormalities, hearing loss, and joint problems.
Contents |
[edit] Types
Genetic changes are related to the following types of Stickler syndrome:
- Stickler syndrome, COL11A1
- Stickler syndrome, COL11A2
- Stickler syndrome, COL2A1
Whether there are two or three types of Stickler syndrome is controversial. Each type is presented here according to the gene involved. The classification of these conditions is changing as researchers learn more about the genetic causes.
[edit] Causes
The syndrome is thought to arise from a mutation of several collagen genes during fetal development. It is a sex independent autosomal dominant trait meaning a person with the syndrome has a 50% chance of passing it on to each child. There are three variants of Stickler syndrome, each associates with a collagen biosynthesis gene.
[edit] Who gets Stickler syndrome?
Stickler syndrome is an autosomal dominant condition, meaning only one parent needs to have an abnormal gene for the child to inherit the disease.
A person with Stickler syndrome has a 50% chance for each pregnancy of passing this mutation on to the child.
For some people, the Stickler syndrome gene mutation is inherited from a parent.
[edit] Symptoms
Individuals with Stickler syndrome experience a range of signs and symptoms. Some people have almost no signs and symptoms; others have all of the features described below. In addition, each feature of this syndrome may vary from subtle to severe.
A characteristic feature of Stickler syndrome is a somewhat flattened facial appearance. This is caused by underdeveloped bones in the middle of the face, including the cheekbones and the bridge of the nose. A particular group of physical features, called the Pierre Robin sequence, is common in children with Stickler syndrome. Robin sequence includes a U-shaped cleft palate (an opening in the roof of the mouth) with a tongue that is too large for the space formed by the small lower jaw. Children with a cleft palate are also prone to frequent ear infections and swallowing difficulties.
Many people with Stickler syndrome are very nearsighted (described as having high myopia) because of the shape of the eye. People with eye involvement are prone to increased pressure within the eye (glaucoma) and tearing of the lining of the eye (retinal detachment). The jelly-like substance within the eye (the vitreous) has a distinctive appearance in the types of Stickler syndrome associated with the COL2A1 and COL11A1 genes. The type of Stickler syndrome associated with the COL11A2 gene does not affect the eye.
Another sign of Stickler syndrome is mild to severe hearing loss that, for some people, may be progressive (see hearing loss with craniofacial syndromes). The joints of affected children and young adults may be very flexible (hypermobile). Arthritis often appears at an early age and worsens as a person gets older. Learning difficulties can also occur because of hearing and sight impairments.
[edit] Notable people with Stickler syndrome
Ben Quinlan [verification needed]
[edit] Genetics
Mutations in the COL11A1, COL11A2 and COL2A1 genes cause Stickler syndrome. These genes are involved in the production of type II and type XI collagen. Collagens are complex molecules that provide structure and strength to connective tissue (the tissue that supports the body's joints and organs). Mutations in any of these genes disrupt the production, processing, or assembly of type II or type XI collagen. Defective collagen molecules or reduced amounts of collagen affect the development of bones and other connective tissues, leading to the characteristic features of Stickler syndrome.
Other, as yet unknown, genes may also cause Stickler syndrome because not all individuals with the condition have mutations in one of the three identified genes.
[edit] Scientists involved
Scientists associated with the discovery of this syndrome include:
- B. David
- Pierre Robin
- Gunnar B. Stickler
- Hans Wagner
- G. Weissenbacher
- Ernst Zweyműller
[edit] Treatment
Many professionals are likely to be involved in the treatment of those with Stickler's Syndrome, including ophthalmologists, audiologists and rheumatologists.
[edit] Epidemiology
Overall, the estimated prevalence of Stickler syndrome is about 1 in 10,000 people.
[edit] See also
- Mandy Haberman, inventor of the Haberman Feeder when her daughter, born with Stickler syndrome, required special feeding due to cleft palate.
[edit] References
- Admiraal RJ, Szymko YM, Griffith AJ, Brunner HG, Huygen PL (2002). "Hearing impairment in Stickler syndrome". Adv Otorhinolaryngol 61: 216-23. PMID 12408087.
- Annunen S, Korkko J, Czarny M, Warman ML, Brunner HG, Kaariainen H, Mulliken JB, Tranebjaerg L, Brooks DG, Cox GF, Cruysberg JR, Curtis MA, Davenport SL, Friedrich CA, Kaitila I, Krawczynski MR, Latos-Bielenska A, Mukai S, Olsen BR, Shinno N, Somer M, Vikkula M, Zlotogora J, Prockop DJ, Ala-Kokko L (1999). "Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes". Am J Hum Genet 65 (4): 974-83. PMID 10486316.
- Liberfarb RM, Levy HP, Rose PS, Wilkin DJ, Davis J, Balog JZ, Griffith AJ, Szymko-Bennett YM, Johnston JJ, Francomano CA, Tsilou E, Rubin BI (2003). "The Stickler syndrome: genotype/phenotype correlation in 10 families with Stickler syndrome resulting from seven mutations in the type II collagen gene locus COL2A1". Genet Med 5 (1): 21-7. PMID 12544472.
- Nowak CB (1998). "Genetics and hearing loss: a review of Stickler syndrome". J Commun Disord 31 (5): 437-53; 453-4. PMID 9777489.
- Parke DW (2002). "Stickler syndrome: clinical care and molecular genetics". Am J Ophthalmol 134 (5): 746-8. PMID 12429253.
- Richards AJ, Baguley DM, Yates JR, Lane C, Nicol M, Harper PS, Scott JD, Snead MP (2000). "Variation in the vitreous phenotype of Stickler syndrome can be caused by different amino acid substitutions in the X position of the type II collagen Gly-X-Y triple helix". Am J Hum Genet 67 (5): 1083-94. PMID 11007540.
- Snead MP, Yates JR (1999). "Clinical and Molecular genetics of Stickler syndrome". J Med Genet 36 (5): 353-9. PMID 10353778.
- ↑ STICKLER GB, BELAU PG, FARRELL FJ, JONES JD, PUGH DG, STEINBERG AG, WARD LE (1965). "HEREDITARY PROGRESSIVE ARTHRO-OPHTHALMOPATHY". Mayo Clin Proc 40: 433-55. PMID 14299791.
[edit] External links
- Information about Stickler Syndrome from Seattle Children's Craniofacial Center
- UK Stickler Syndrome Support Group
- Vision Support Guide
- US Stickler Syndrome Support Group
