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5,854 Possible Causes for Bone-Spicule Pigmentation in Peripheral Retinal Pigment Epithelium, Epilepsy, Mutation in the TTLL5 Gene

  • Neuronal Ceroid Lipofuscinosis 4B

    Infantile and late-infantile retinal findings include fine retinal pigment epithelium pigment atrophy with no bone spicule changes and disk pallor.[journals.lww.com] […] a patient with a possible metabolic epilepsy "[books.google.com] Core symptoms of these conditions typically include epilepsy, cognitive decline and visual failure.[books.google.com]

    Missing: Mutation in the TTLL5 Gene
  • Stroke

    Our primary aim was to evaluate whether early EEG abnormalities can predict poststroke epilepsy.[onlinelibrary.wiley.com] Patients with a history of epilepsy before the stroke (n 19) or who died in the first day after the stroke (n 17) were excluded from these analyses.[bmj.com] The primary outcome was the occurrence of at least one unprovoked seizure (poststroke epilepsy).[onlinelibrary.wiley.com]

    Missing: Bone-Spicule Pigmentation in Peripheral Retinal Pigment Epithelium Mutation in the TTLL5 Gene
  • Status Epilepticus

    We report the first case of epilepsy surgery in a liver-transplanted patient with refractory temporal lobe epilepsy.[ncbi.nlm.nih.gov] In both fields of epilepsy and status epilepticus, the most frequently cited journal was Epilepsia (26 articles on epilepsy and 19 articles on status epilepticus).[ncbi.nlm.nih.gov] Copyright 2018 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.[ncbi.nlm.nih.gov]

    Missing: Bone-Spicule Pigmentation in Peripheral Retinal Pigment Epithelium Mutation in the TTLL5 Gene
  • Chronic Fatigue Syndrome

    Virus in brain of child with hemiplegia, hemiconvulsions, and epilepsy. Lancet. 1977; 2 666 63 Walter G F, Renella R R.[doi.org] Vicky Whittemore is an epilepsy researcher recently tasked with overseeing CFS-ME research at the National Institute of Neurological Disorders and Stroke, and a member of[gizmodo.com] ., multiple sclerosis, neuromuscular diseases, epilepsy or other diseases requiring ongoing medication that could cause fatigue, stroke, head injury with residual neurologic[doi.org]

    Missing: Bone-Spicule Pigmentation in Peripheral Retinal Pigment Epithelium Mutation in the TTLL5 Gene
  • Generalized Motor Seizure

    A case is reported in which a Nucleus 22 channel intracochlear implant was used to treat a deaf Hungarian woman (aged 37 years) with a 34-year history of grand mal (GM) epilepsy[ncbi.nlm.nih.gov] Abstract In a controlled clinical investigation based on 14 patients with focal seizures and 3 patients with secondary generalized grand mal epilepsy, all with insufficient[ncbi.nlm.nih.gov] Abstract Interictal EEG records of Nigerian epileptic patients living in Lagos and clearly diagnosed as having grand mal epilepsy were compared with those of British epileptic[ncbi.nlm.nih.gov]

    Missing: Bone-Spicule Pigmentation in Peripheral Retinal Pigment Epithelium Mutation in the TTLL5 Gene
  • Absence Seizure

    Our Mission The mission of the Epilepsy Foundation is to lead the fight to overcome the challenges of living with epilepsy and to accelerate therapies to stop seizures, find[epilepsyfoundation.org] The definition of epilepsy is more than one seizure. The frequency of seizures in people with epilepsy varies.[patient.info] For more information, see the separate leaflets called Epilepsy and Seizures and Types of Epilepsy and Seizures . What is an absence seizure?[patient.info]

    Missing: Bone-Spicule Pigmentation in Peripheral Retinal Pigment Epithelium Mutation in the TTLL5 Gene
  • Subdural Hematoma

    CONCLUSIONS: In case of refractory treatment of epilepsy, dislocation of pacemaker electrodes is a, most certainly, rare but possible differential diagnosis.[ncbi.nlm.nih.gov] As many as 10 percent of patients had a history of alcoholism or epilepsy, the Welsh team reported.[well.blogs.nytimes.com] […] hematoma following surgey Spontaneous Risk factors for chronic subdural hematoma include the following: Diabetes Thrombocytopenia Cardiovascular disorder Arachnoid cyst Epilepsy[symptoma.com]

    Missing: Bone-Spicule Pigmentation in Peripheral Retinal Pigment Epithelium Mutation in the TTLL5 Gene
  • Rolandic Epilepsy

    Benign Rolandic epilepsy or benign childhood epilepsy with centrotemporal spikes (BCECTS) is the most common epilepsy syndrome in childhood.[en.wikipedia.org] Rolandic epilepsy, sometimes also referred to as benign childhood epilepsy with centrotemporal spikes, is the most common type of childhood epilepsy.[symptoma.com] Abstract Benign childhood epilepsy with centrotemporal spikes (BCECTS) is an idiopathic focal epilepsy syndrome, the benign characteristics of which are debated; in fact,[ncbi.nlm.nih.gov]

    Missing: Bone-Spicule Pigmentation in Peripheral Retinal Pigment Epithelium Mutation in the TTLL5 Gene
  • Medial Sclerosis

    Mesial temporal sclerosis can cause a type of epilepsy called temporal lobe epilepsy.[inova.org] In the majority of cases, there may be no cause that can be discovered for epilepsy.[hopkinsmedicine.org] […] sclerosis, hippocampal epilepsy, temporal lobe epilepsy with hippocampal sclerosis, medial temporal lobe epilepsy, MTLE, temporal lobe epilepsy, limbic epilepsy, psychomotor[medlink.com]

    Missing: Bone-Spicule Pigmentation in Peripheral Retinal Pigment Epithelium Mutation in the TTLL5 Gene
  • Aspiration Pneumonia

    Epilepsy. Coma. Critical illnesses and debilitated patients. Gastroesophageal reflux disease (GERD).[healthhype.com]

    Missing: Bone-Spicule Pigmentation in Peripheral Retinal Pigment Epithelium Mutation in the TTLL5 Gene

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