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Results 1 - 10 of 55 for CK syndrome
  1. NSDHL gene 
    ... Condition Variants in the NSDHL gene can cause CK syndrome, a condition characterized by intellectual disabilities and behavior ... of females) who have a variant that causes CK syndrome are typically unaffected; however, some may experience mild ...
    https://medlineplus.gov/genetics/gene/nsdhl - Genetics
  2. Klippel-Trenaunay syndrome 
    ... PubMed Kihiczak GG, Meine JG, Schwartz RA, Janniger CK. Klippel-Trenaunay syndrome: a multisystem disorder possibly resulting from a pathogenic ...
    https://medlineplus.gov/.../condition/klippel-trenaunay-syndrome - Genetics
  3. Larsen syndrome 
    ... Feb 29. Citation on PubMed Sajnani AK, Yiu CK, King NM. Larsen syndrome: a review of the literature and case report. ...
    https://medlineplus.gov/genetics/condition/larsen-syndrome - Genetics
  4. Myoclonic epilepsy with ragged-red fibers 
    ... HA, Munhoz RP, Muzzio JA, Scola RH, Kay CK, Raskin S, Werneck LC, Bruhn H. Cerebellar ataxia, myoclonus, cervical lipomas, and MERRF syndrome. Case report. Mov Disord. 2008 Jun 15;23( ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  5. Pericarditis - after heart attack 
    ... often does occur in some people with Dressler syndrome. Tests may include: Cardiac injury markers (CK-MB and troponin may help tell pericarditis from ...
    https://medlineplus.gov/ency/article/000166.htm - Medical Encyclopedia
  6. Noonan syndrome 
    ... SYNDROME 6; NS6 NOONAN SYNDROME 9; NS9 NOONAN SYNDROME 10; NS10 PubMed Chen PC, Yin J, Yu HW, Yuan T, Fernandez M, Yung CK, Trinh QM, Peltekova VD, Reid JG, Tworog-Dube ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  7. EPCAM gene 
    ... Hoenselaar E, Hendriks-Cornelissen SJ, Tsui WY, Kong CK, Brunner HG, van Kessel AG, Yuen ST, van Krieken JH, Leung SY, Hoogerbrugge N. Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of ...
    https://medlineplus.gov/genetics/gene/epcam - Genetics
  8. Lynch syndrome 
    ... Hoenselaar E, Hendriks-Cornelissen SJ, Tsui WY, Kong CK, Brunner HG, van Kessel AG, Yuen ST, van Krieken JH, Leung SY, Hoogerbrugge N. Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of ...
    https://medlineplus.gov/genetics/condition/lynch-syndrome - Genetics
  9. Enlarged Vestibular Aqueduct (EVA) (Vestibular Disorders Association)  
    Enlarged Vestibular Aqueduct is a condition caused by a malformation in the inner ear that leads to loss of hearing and vestibular function. ... Dizziness ...
    https://vestibular.org/.../enlarged-vestibular-aqueduct-eva - External Health Links
  10. Magnets for Pain From the National Institutes of Health (National Center for Complementary and Integrative Health)  
    Wrist Injuries and Disorders/Treatments and Therapies ... Wrist Injuries and Disorders ... Complementary and Integrative Medicine/Specifics ... Complementary and Integrative ...
    https://www.nccih.nih.gov/.../magnets-for-pain-what-you-need-to-know - External Health Links
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