waardenburg syndrome การใช้

• Whether or not this is a result of Waardenburg syndrome remains unclear.
• About 1 in 30 students in schools for the deaf have Waardenburg syndrome.
• The shortage of melanocytes causes some of the characteristic features of Waardenburg syndrome.
• Mutations in either gene are links to Waardenburg syndrome.
• This helped them distinguish forms of Waardenburg syndrome.
• Autosomal dominant congenital hearing loss can be attributed to such causes like Waardenburg Syndrome.
• Waardenburg syndrome is a rare genetic disorder.
• Mutations in the EDNRB gene are associated with ABCD syndrome and some forms of Waardenburg syndrome.
• For example, mutations of MITF have been implicated in both Waardenburg syndrome and Tietz syndrome.
• Other genetic syndromes occasionally associated with widow's peaks include Waardenburg syndrome and Aarskog syndrome.
• Waardenburg syndrome type 2 ( WS type 2 ) in humans is also a type of microphthalmia syndrome.
• Mutations in the EDN3, EDNRB, MITF, PAX3, SNAI2, and SOX10 genes are implicated in Waardenburg Syndrome.
• Enzo MacLeod, protagonist of Peter May's series " The Enzo Files ", has Waardenburg syndrome.
• Scientists believe they have a clearer picture of the role of transcription factors in a condition known as Type 1 Waardenburg syndrome.
• This helped scientists discover that it is the same as type IV Waardenburg syndrome, also known as Shah-Waardenburg Syndrome.
• This helped scientists discover that it is the same as type IV Waardenburg syndrome, also known as Shah-Waardenburg Syndrome.
• Dutch ophthalmologist Petrus Johannes Waardenburg ( 1886 1979 ) brought about the idea of Waardenburg syndrome when he examined two deaf twins.
• Mutations in Pax3 can cause a variety of complications including Waardenburg syndrome I and III as well as craniofacial-deafness-hand syndrome.
• Syndromic cases occur with diseases such as Usher syndrome, Stickler syndrome, Waardenburg syndrome, Alport's syndrome, and neurofibromatosis type 2.
• Waardenburg syndrome is most often associated with congenital disorders involving the intestinal tract and spine, an elevation of the scapula, among other symptoms.