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55 Possible Causes for Angiomyolipoma, Nocturnal Seizure

  • Tuberous Sclerosis

    OBJECTIVE: To examine temporal relationships between tuberous sclerosis complex (TSC) and renal angiomyolipoma diagnosis and outcomes, treatment, and healthcare utilization[ncbi.nlm.nih.gov] Renal angiomyolipomas are rare type of benign renal neoplasm.[ncbi.nlm.nih.gov] Renal angiomyolipoma (AML) is the most commonly encountered mesenchymal tumor of the kidney which can present spontaneously or in association with tuberous sclerosis complex[ncbi.nlm.nih.gov]

  • Focal Onset Impaired Awareness Seizure

    […] 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] Most SUDEPs occur after one or more seizure(s) during sleep. Nocturnal seizures may go unrecognized.[ncbi.nlm.nih.gov] Generalised seizures Partial seizures Nocturnal seizures Status epilepticus What are seizure triggers? Does everyone get warning signs before a seizure?[irishhealth.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] […] epileptic seizures using wireless 3-D accelerometer sensors , (2014) . 237 242 7001847 , 10.1109/HealthCom.2014.7001847 Ying Chang, Li-ya Yang, Meng-chao Zhang and Song-Yan[doi.org]

  • 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] Página 112 - JC (1998) Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24. Am. J. Hum.[books.google.es]

  • Hereditary Hyperekplexia

    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] […] spasm, exaggerated startle response and fetal posture with flexion of forearm and legs, clenched fists, and anxious stare. 3 The tonic spasms may mimic generalised tonic seizures[pmj.bmj.com]

  • Budd-Chiari Syndrome

    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] Patient 6 was diagnosed with paroxysmal nocturnal haemoglobinuria with severe episodic intravascular haemolysis requiring blood transfusion support and serial partial red[journals.lww.com]

  • Familial Infantile Bilateral Striatal Necrosis

    angiomyolipoma Membranoproliferative glomerulonephritis Henoch-Schonlein purpura nephritis Reproductive system diseases Reproductive system disease 46,XY disorders of sex[csirnotes.com] ) Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) Idiopathic generalied epilepsies (IGEs) Autosomal dominant temporal lobe epilepsy (ADTLE) Progressive myoclonic[csirnotes.com] […] deposits (GFND) Hyperglycinuria Diabetic nephropathy Lupus nephritis Interstitial cystitis (IC) IgA nephropathy Renal anemia Rapidly progressive glomerulonephritis (RPGN) Renal[csirnotes.com]

  • Autosomal Agammaglobulinemia

    Associated with adenoma sebaceum (facial lesion), myocardial rhabdomyomas, renal angiomyolipomas.[kumc.edu] Parkinsonism, Autosomal Recessive Infantile Spasm Syndrome-2, X-linked Juvenile Myoclonic Epilepsy Lafora Disease MASA Syndrome Microcephaly with Early-Onset Intractable Seizures[estudiosgeneticos.com.ar] Delay (MCSZ) Mowat-Wilson Syndrome Mucolipidosis IV Nemaline Myopathy Neuronal Ceroid Lipofuscinoses (NCL) Niemann-Pick Disease, Type C Niemann-Pick Disease, Types A and B Nocturnal[estudiosgeneticos.com.ar]

  • 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] nocturnal frontal lobe epilepsy (ADNFLE) [PATH: hsa04080 hsa04725 ] H00808 Idiopathic generalized epilepsies [PATH: hsa04727 hsa04010 ] H02215 Childhood absence epilepsy[genome.jp] angiomyolipoma [PATH: hsa04150 ] H01726 Membranoproliferative glomerulonephritis [PATH: hsa04610 ] H01767 Henoch-Schonlein purpura nephritis H02011 Familial juvenile hyperuricemic[genome.jp]

  • Neurofibromatosis Type 6

    angiomyolipoma glioma juvenile pilocytic astrocytoma ( 20% of patients) 13 optic nerve glioma diffuse brainstem glioma spinal astrocytoma and spinal pilocytic astrocytoma[radiopaedia.org] […] epilepsy – ADFNLE : Cholinergic receptor, nicotinic, alpha 4 ( CHR- NA4 ) and Cholinergic receptor, nicotinic, beta 2 ( CHRNB2 ) genes; Epilepsy, generalized, with febrile seizures[isn.cnr.it] […] associated with increased incidence of numerous tumors 1-6 : pheochromocytoma malignant peripheral nerve sheath tumor (MPNST) ( 10% of patients) 7 Wilms tumor rhabdomyosarcoma renal[radiopaedia.org]

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