Search:
Go
English
Deutsch
Français
Japanese
Chinese Simplified
Chinese Traditional
Korean
Russian
Arabic
Česky
Greek
Italiano
Afrikaans
Aragonés
Armenian
Asturianu
Azerbaijani
Bahasa Indonesia
Bahasa Melayu
Bangla
Bashkir
Belarusian
Bosanski
Brezhoneg
Bulgarian
Català
Cymraeg
Dansk
Eesti
Español
Esperanto
Euskara
Frysk
Furlan
Føroyskt
Gaeilge
Gàidhlig
Galego
Gujarati
Hebrew
Hindi
Hrvatski
Interlingua
Íslenska
Kannada
Kaszëbsczi
Kazakh
Kiswahili
Kurdî
Kyrgyz
Latviski
Lëtzebuergesch
Lietuvių
Lingua Latina
Magyar
Makedonski
Marathi
Nederlands
Nordfriisk
Norsk
O'zbekcha
Occitan
Ossetian
Persian
Polski
Português
Punjabi Gurmukhi
Română
Rumantsch
Sardu
Seeltersk
Shqip
Sicilianu
Sinhala
Slovensko
Slovensky
Srpski
Suomi
Svenska
Tagalog
Taiwanese
Tamil
Tatarça
Telugu
Thai
Tiếng Việt
Türkçe
Türkmençe
Ukrainian
Urdu
Uyghurche
DMOZ Internet Directory
Presented by
DMOZLive.com
Home
About
Submit Site
Tweet
Home
Health
Conditions and Diseases
Congenital Anomalies
Craniofacial Anomalies
Stickler's Syndrome
8 Sites
Stickler's Syndrome is a disorder affecting collagen, characterized by distinctive facial abnormalities, eye problems, hearing loss and joint problems.
Sites
[ Submit ]
Wikipedia: Stickler Syndrome
- Encyclopedia article on this condition, the types, causes, symptoms, genetics, treatment and epidemiology.
Genetics Home Reference: Stickler Syndrome
- Stickler syndrome is a group of hereditary conditions characterized by a distinctive facial appearance, eye abnormalities, hearing loss and joint problems. Describes the condition and discusses how it is inherited.
Seattle Children's Hospital: Stickler Syndrome
- Provides an overview of this genetic disorder of connective tissue, the symptoms, diagnosis and treatment.
National Organization for Rare Disorders: Stickler Syndrome
- NORD provides information on this genetic disorder and the genes concerned. Includes links to organizations.
Medic8: Stickler Syndrome
- Article describing this syndrome and providing information on the defective genes involved in the production of type II and type XI collagen.
Mayo Clinic: Stickler Syndrome
- Provides an overview of this rare inherited disorder including symptoms, causes, risk factors, complications and treatment.
OMIM: Stickler Syndrome, Type 1
- Abstracts from various research studies on the membranous vitreous type of this syndrome.
OMIM: Stickler Syndrome Type 2
- Abstracts from various studies on the beaded vitreous type of this syndrome.
Click
[ Submit ]
above to Add a New Site, Update a Site, or Remove a Site from this Category.
See Also
Genetic Disorders
Health : Conditions and Diseases
331 Sites
Rare Disorders
Health : Conditions and Diseases
7 Sites
This directory is made available through a Creative Commons Attribution license from the
DMOZ Organization.