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81 Possible Causes for Angiomyolipoma, Heart Disease, Nocturnal Seizure

  • Tuberous Sclerosis

    ACC/AHA 2008 guidelines for the management of adults with congenital heart disease: a report of the American College of Cardiology/American Heart Association task force on[doi.org] OBJECTIVE: To examine temporal relationships between tuberous sclerosis complex (TSC) and renal angiomyolipoma diagnosis and outcomes, treatment, and healthcare utilization[ncbi.nlm.nih.gov] It is also associated with cortical tuber and hamartomas formation throughout the body, especially the heart, kidneys, and eyes.[icd9data.com]

  • Temporal Lobe Epilepsy

    […] astrocytoma White matter abnormalities Tuberous sclerosis or Bourneville's disease is an inherited condition characterized by the presence of hamartomas in many organs including angiomyolipoma[radiologyassistant.nl] Pagina 112 - JC (1998) Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24. Am. J. Hum.[books.google.ro] Studies have shown that believers live longer, are healthier, even that they may have lower levels of cancer and heart disease.[bbc.co.uk]

  • Familial Progressive Myoclonic Epilepsy

    TODPD 300244 Genetic Test Registry Tuberous Sclerosis 1 Tuberose Sclerosis Tuberous Sclerosis Complex TSC1 TS TSC 191100 Genetic Test Registry Tuberous Sclerosis 2 Tsc2 Angiomyolipomas[ukgtn.nhs.uk] […] infancy Familial Frontal lobe epilepsies (Autosomal Dominant Nocturnal Familial Frontal lobe Epilepsy) Familial Mesial Temporal lobe epilepsies Familial Lateral Temporal[swedish.org] A statement for healthcare professionals from a special writing group of the Stroke Council, American Heart Association.[books.google.es]

  • Hereditary Hyperekplexia

    Pulmonary Hypertension Congenital Heart Disease Newborn Disease – Childhood Disease – Adulthood Disease The skin is the largest organ in the body, serving as a protective[genomicinterpretation.org] TODPD 300244 Genetic Test Registry Tuberous Sclerosis 1 Tuberose Sclerosis Tuberous Sclerosis Complex TSC1 TS TSC 191100 Genetic Test Registry Tuberous Sclerosis 2 Tsc2 Angiomyolipomas[ukgtn.nhs.uk] […] plus PS604233 Epilepsy, nocturnal frontal lobe PS600513 Epilepsy, progressive myoclonic PS254800 Epileptic encephalopathy, early infantile PS308350 Epileptic encephalopathy[omim.org]

  • Microcephalic Primordial Dwarfism due to ZNF335 Deficiency

    disease syndrome 2 Cases 423306 Microcephaly-short stature- intellectual disability-facial dysmorphism syndrome 2 Cases 397951 Microcephaly-thin corpus callosum-intellectual[azkurs.org] {TSC2 angiomyolipomas, renal, modifier of}, 613254 (3) IFNG G:147570 . {Tuberculosis, protection against}, 607948 (3) IFNGR1 G:107470 .[usegalaxy.org] Paroxysmal nocturnal hemoglobinuria 2 615399 610272 Autosomal dominant; Somatic mutation PIGT 20q13.12 Multiple congenital anomalies-hypotonia-seizures syndrome 3 615398 610272[mnglabs.com]

  • Autosomal Dominant Coronary Artery Disease 1

    This brand-new companion to Braunwald's Heart Disease was designed as a stand-alone reference for physicians treating patients who present with complex, unique challenges,[books.google.com] Associated with adenoma sebaceum (facial lesion), myocardial rhabdomyomas, renal angiomyolipomas.[kumc.edu] , or nocturnal agonal respirations.[geneticheartdisease.org]

  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    Associated syndromes: congenital heart disease, leukemia, premature Alzheimer's disease (same morphological changes).[kumc.edu] Other manifestations such as dementia, dystonia, and seizures are less common.[neuroweb.us] If the trinucleotide repeat is long, vision loss can actually come on first In childhood, seizures and heart disease come on with ataxia and vision loss.[verywell.com]

  • Malignant Atrophic Papulosis

    Birt-Hogg-Dub syndrome with renal angiomyolipoma. Intern Med 2012; 51: 1279-1280.40. Coleman JA, Russo R. Hereditary and familial kidney cancer.[vdocuments.net] Epileptic seizures,Nocturnal enuresis, ADD. Chiropractic Pediatrics Vol 1 No. 1, April, 1994.[alonsoquiropractica.com] Prevention of coronary heart disease with pravastatin in men with hypercholesterolemia. ‏[books.google.com]

  • Budd-Chiari Syndrome

    Scimitar syndrome is a congenital heart disease characterized by an abnormal drainage of the right lung into the inferior vena cava, the right atrium or a variety of venous[ncbi.nlm.nih.gov] A 55-year-old man with a history of chronic hepatitis B infection and alcoholism had undergone previously a left lateral segmentectomy for hepatic epitheloid angiomyolipoma[ncbi.nlm.nih.gov] He developed seizures secondary to sagittal sinus thrombosis. He also had antiphospholipid syndrome.[journals.lww.com]

  • Intestinal Pseudo-Obstruction - Patent Ductus Arteriosus - Natal Teeth

    : hsa04974 hsa04978 ] H01500 Lupus nephritis H01551 Interstitial cystitis H01581 IgA nephropathy H01642 Renal anemia H01688 Rapidly progressive glomerulonephritis H01691 Renal[genome.jp] […] block * Congenital heart disease ptosis hypodontia craniostosis * Congenital heart disease radio ulnar synostosis mental retardation * Congenital heart septum defect * Congenital[medicalgeek.com] disease, etc.).[pongpdf.com]

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