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Results 1 - 10 of 23 for Reynolds syndrome
  1. Nephrotic Syndrome in Children From the National Institutes of Health (National Institute of Diabetes and Digestive and Kidney Diseases)  
    Overview of nephrotic syndrome in children, a combination of symptoms that can develop when a child’s kidneys are not working properly. ... Childhood nephrotic ...
    https://www.niddk.nih.gov/.../children/nephrotic-syndrome-children - External Health Links
  2. X chromosome 
    ... Davis S, Hench A, Nimishakavi S, Beauregard R, Reynolds A, Fenton L, Albrecht L, Ross J, Visootsak J, Hansen R, Hagerman R. A new look at XXYY syndrome: medical and psychological features. Am J Med Genet ...
    https://medlineplus.gov/genetics/chromosome/x - Genetics
  3. 48,XXYY syndrome 
    ... Davis S, Hench A, Nimishakavi S, Beauregard R, Reynolds A, Fenton L, Albrecht L, Ross J, Visootsak J, Hansen R, Hagerman R. A new look at XXYY syndrome: medical and psychological features. Am J Med Genet ...
    https://medlineplus.gov/genetics/condition/48xxyy-syndrome - Genetics
  4. Y chromosome 
    ... Davis S, Hench A, Nimishakavi S, Beauregard R, Reynolds A, Fenton L, Albrecht L, Ross J, Visootsak J, Hansen R, Hagerman R. A new look at XXYY syndrome: medical and psychological features. Am J Med Genet ...
    https://medlineplus.gov/genetics/chromosome/y - Genetics
  5. 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
  6. Neurofibromatosis type 1 
    ... j.spen.2006.01.006. Citation on PubMed Reynolds RM, Browning ... Rose VM. Neurocutaneous syndromes. Mo Med. 2004 Mar-Apr;101(2):112- ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-1 - Genetics
  7. Pendred syndrome 
    ... Zalewski CK, Muskett J, Chattaraj P, Shawker T, Reynolds JC, Butman JA, Brewer CC, ... Syndrome (PDS/SLC26A) gene: an increasingly complex phenotypic spectrum ...
    https://medlineplus.gov/genetics/condition/pendred-syndrome - Genetics
  8. SLC26A4 gene 
    ... Zalewski CK, Muskett J, Chattaraj P, Shawker T, Reynolds JC, Butman JA, Brewer CC, ... Syndrome (PDS/SLC26A) gene: an increasingly complex phenotypic spectrum ...
    https://medlineplus.gov/genetics/gene/slc26a4 - Genetics
  9. How Is Pelvic Pain Treated? From the National Institutes of Health (Eunice Kennedy Shriver National Institute of Child Health and Human Development)  
    Pelvic Pain/Treatments and Therapies ... Pelvic Pain ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... Treatment depends on the ...
    https://www.nichd.nih.gov/.../pelvicpain/conditioninfo/treatments - External Health Links
  10. CDH23 gene 
    ... mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes. J Med Genet. 2011 Nov;48(11):767-75. doi: 10.1136/jmedgenet-2011-100262. Epub 2011 Sep 22. Citation on PubMed Siemens J, Lillo C, Dumont RA, Reynolds A, Williams DS, Gillespie PG, Muller U. Cadherin ...
    https://medlineplus.gov/genetics/gene/cdh23 - Genetics
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