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1,194 Possible Causes for Sclerocornea, Spontaneous Rupture of Membranes, Tricuspid Valve Insufficiency

  • Brittle Cornea Syndrome Type 2

    Valve Insufficiency Ebstein Anomaly NEXN Nexilin Dilated Cardiomyopathy 1CC (CMD1CC) Familial Hypertrophic Cardiomyopathy Type 20 NF1 Neurofibromin 1 Congenital Heart Diseases[bcm.edu] Problems during delivery Due to the fragility of connective tissue, those with EDS are more prone to prelabour spontaneous rupture of membranes (SROM), including preterm SROM[patient.info] […] cornea ; Gait disturbance ; Hearing impairment ; Inguinal hernia ; Joint hypermobility ; Keratoconus ; Keratoglobus ; Megalocornea ; Myalgia ; Myopia ; Recurrent fractures ; Sclerocornea[mousephenotype.org]

  • Ehlers-Danlos Syndrome

    valve insufficiency often complicating with "true" mitral valve prolapse in the ecocardiographic study.[ncbi.nlm.nih.gov] Problems during delivery Due to the fragility of connective tissue, those with EDS are more prone to prelabour spontaneous rupture of membranes (SROM), including preterm SROM[patient.info] valve insufficiency often complicating with “true” mitral valve prolapse in the ecocardiographic study.[doi.org]

    Missing: Sclerocornea
  • Isolated Congenital Sclerocornea

    Acute ruptures of Descemet membrane or acute hydrops may occur, leading to corneal edema that often resolves spontaneously, leaving stromal scarring.[doctorlib.info] Homepage Rare diseases Search Search for a rare disease Isolated congenital sclerocornea ORPHA:91490 Synonym(s): - Prevalence: - Inheritance: - Age of onset: - ICD-10: Q13.3[orpha.net] The extent of the resulting opacity varies from peripheral to total (sclerocornea totalis).[en.wikipedia.org]

    Missing: Tricuspid Valve Insufficiency
  • Congenital Heart Disease

    Tricuspid (systemic) valve insufficiency is often also an important component in the development of heart failure.[doi.org] Approximately 17% to 21% of all patients with CHD ultimately deliver preterm as a result of either spontaneous preterm labor/preterm premature rupture of membranes (59%) or[doi.org]

    Missing: Sclerocornea
  • Familial Congenital Nasolacrimal Duct Obstruction

    Atresia Tricuspid Valve Insufficiency Tricuspid Valve Prolapse Tricuspid Valve Stenosis Trigeminal Nerve Diseases Trigeminal Neuralgia Trilogy of Fallot Trismus Trisomy Trochlear[medgene.med.harvard.edu] rupture of membranes (1) Thyroid disease in pregnancy (1) Transdermal contraception (1) Vaginal birth after cesarean (1) Vaginal bleeding (1) Vaginal smears (17) Hematologic[innovations.ahrq.gov] Congenital glaucoma, nystagmus, cataracts, lacrimal duct obstruction (37%), ptosis (29%), colobomas and numerous corneal abnormalities including keratoglobus, sclerocornea[disorders.eyes.arizona.edu]

  • Congestive Heart Failure

    Secondary changes in valve function, particularly the severity of mitral and tricuspid valve insufficiency, should be determined.[doi.org] Secondary changes, particularly the severity of mitral and tricuspid valve insufficiency, should be determined.[doi.org] All valves should be evaluated for anatomic and flow abnormalities to exclude the presence of primary valve disease.[doi.org]

    Missing: Sclerocornea Spontaneous Rupture of Membranes
  • Heart Failure

    Secondary changes in valve function, particularly the severity of mitral and tricuspid valve insufficiency, should be determined.[doi.org] Secondary changes, particularly the severity of mitral and tricuspid valve insufficiency, should be determined.[doi.org] All valves should be evaluated for anatomic and flow abnormalities to exclude the presence of primary valve disease.[doi.org]

    Missing: Sclerocornea Spontaneous Rupture of Membranes
  • Congenital Primary Aphakia

    Unfortunately, these cases often develop glaucoma, and the natural history is that when untreated, they will often spontaneously rupture. 38 This author tried to place an[journals.lww.com] Conclusions: : Two novel families with the sclerocornea-aphakia complex due to FOXe3 mutations are presented.[iovs.arvojournals.org] In some cases, CPA can be associated with other eye abnormalities including microphthalmia, absence of the iris, anterior segment aplasia, and/or sclerocornea (when the cornea[checkorphan.org]

    Missing: Tricuspid Valve Insufficiency
  • Cardiomyopathy

    Cardiomyopathy can be acquired or inherited. “Acquired” means you aren’t born with the disease, but you develop it due to another disease, condition, or factor. “Inherited” means your parents passed the gene for the disease on to you. Researchers continue to look for the genetic links to cardiomyopathy and to[…][web.archive.org]

    Missing: Sclerocornea Spontaneous Rupture of Membranes
  • Coronary Atherosclerosis

    Coronary artery disease (CAD) exhibits the rules of the multifactorial hereditary. Notwithstanding, the role of genetic factors in the prevalence of CAD is estimated very high. SIRT1 plays an athero-protective role and alterations in its expression have some important consequence in the metabolism, cholesterol, and[…][ncbi.nlm.nih.gov]

    Missing: Sclerocornea Spontaneous Rupture of Membranes

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