Create issue ticket

599 Possible Causes for Syndrome, Triple X

  • Trisomy X Syndrome

    What is triple X syndrome? Normally, females have two X chromosomes. Triple X Syndrome occurs when a female has three X chromosomes in her body's cells.[patientslikeme.com] Trisomy X syndrome, or 47, XXX, develops in approximately 1 in 1000 girls but is yet to be diagnosed in many patients.[symptoma.com] Triple X syndrome is a genetic disorder in which a girl has three X chromosomes instead of two. Triple X occurs once in every 1,000 female births.[livestrong.com]

  • Triple A Syndrome

    Triple X syndrome Genetics Home Reference[en.wikipedia.org] Triple A syndrome (Allgrove syndrome) is an autosomal recessive disorder consisting of achalasia, alacrima and Addison insufficiency.[ncbi.nlm.nih.gov] Abstract Triple A syndrome is a rare autosomal recessive disorder characterized by alacrima, achalasia, and adrenal insufficiency.[ncbi.nlm.nih.gov]

  • Five X Syndrome

    General pathology Genetic and developmental anomalies Chromosomal diseases Constitutional trisomies triple X syndrome Definition: Triple X syndrome, also called trisomy X[humpath.com] Mutations in the FOXP3 gene cause IPEX syndrome .[ghr.nlm.nih.gov] Triple X is due to a random event .[reliawire.com]

  • Otitis Media

    […] with ampicillin, triple sulphonamide, erythromycin and placebo ( Howie 1972 ).[doi.org] Woakes' syndrome is characterised by severe recurrent nasal polyps in early childhood with broadening of the nose, nasal dyscrinia, frontal sinus aplasia and bronchiectasis[ncbi.nlm.nih.gov] In comparison to Hurler syndrome (MPS I) and Hunter syndrome (MPS II), characteristic facial and physical features tend to be milder and progression of neurological symptoms[ncbi.nlm.nih.gov]

  • XYY Syndrome

    Triple X females are usually fertile, but sometimes go through the menopause early.[bigpictureeducation.com] […] of XYY syndrome.[symptoma.com] Liebeszeit BU, Rohrer TR, Singer H, Doerr HG: Tall stature as presenting symptom in a girl with triple X syndrome. J Pediatr Endocrinol Metab 2003;16:233–235.[doi.org]

  • 48,XXXY Syndrome

    X y. i bet you didn't even google it, you were just trying to be a smartass. - posted on Feb, 25 2009 @ 02:20 AM Actually, there xxxy is a variant of polysomy X Klinefelter[abovetopsecret.com] However, the features of 48,XXXY syndrome tend to be more severe than those of Klinefelter syndrome and affect more parts of the body.[ghr.nlm.nih.gov] Girls who are born with an extra X chromosome are referred to as having Triple X or Trisomy X.[genetic.org]

  • XXXXY Syndrome

    Y linked: Turner syndrome, Triple X syndrome, Klinefelter's syndrome, XYY syndrome Translocations : Philadelphia chromosome, Burkitt's lymphoma[psychology.wikia.com] Mentally, 49, XXXXY Syndrome males have varying degrees. Many people compare it mentally to Down Syndrome, in that it varies greatly from person to person.[web.archive.org] Y linked Monosomy Turner syndrome (45,X) Trisomy / tetrasomy, other karyotypes / mosaics Klinefelter syndrome (47,XXY) 48,XXYY 48,XXXY 49,XXXYY 49,XXXXY Triple X syndrome[ipfs.io]

  • Ear - Patella - Short Stature Syndrome

    46 Pyoderma Gangrenosum 36 Trisomy 13 Syndrome 47 RothmundThomson Syndrome 37 Trisomy 18 Syndrome 48 Scleromyxedema 38 Syndrome Triple X Syndrome 49 Setleis Syndrome 39 XXY[books.google.com] We report on two brothers with Meier-Gorlin syndrome, the younger of whom was more severely affected.[ncbi.nlm.nih.gov] X Syndrome Zellweger Syndrome[magicfoundation.org]

  • Thrombocytopenia-Absent Radius Syndrome

    46 Pyoderma Gangrenosum 36 Trisomy 13 Syndrome 47 RothmundThomson Syndrome 37 Trisomy 18 Syndrome 48 Scleromyxedema 38 Syndrome Triple X Syndrome 49 Setleis Syndrome 39 XXY[books.google.com] OBJECTIVE: To describe the association of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome and thrombocytopenia-absent radius (TAR) syndrome.[ncbi.nlm.nih.gov] ,XXXYY 49,XXXXY Triple X syndrome (47,XXX) Tetrasomy X (48,XXXX) 49,XXXXX Jacobs syndrome (47,XYY) 48,XYYY 49,XYYYY 45,X/46,XY Translocations Leukemia / lymphoma Lymphoid[en.wikipedia.org]

  • Mayer Rokitansky Kuster Hauser Syndrome

    X karyotype.[ncbi.nlm.nih.gov] The etiology of MRKH syndrome is still largely unknown, probably because of its intrinsic heterogeneity.[ncbi.nlm.nih.gov] In vitro fertilization surrogacy in rare coexisting Mayer-Rokitansky-Kuster-Hauser syndrome and triple X karyotype. Fertil Steril. 2011;95(5):1788.e11–e13. 39.[dovepress.com]

Further symptoms