dee88 - An Overview
dee88 - An Overview
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HelpList of clinical attributes of your condition/phenotype shown from sources such as the Human Phenotype Ontology (HPO) and OMIM. For more info with regard to the disorder, you should Visit the condition details webpage.
Be aware: OMIM is meant to be used principally by medical professionals as well as other industry experts concerned with genetic Issues, by genetics scientists, and by advanced college students in science and drugs. when the OMIM database is get more info open to the general public, people looking for information regarding a private healthcare or genetic situation are urged to refer to with a qualified doctor for analysis and for answers to non-public questions. OMIM® and on the internet Mendelian Inheritance in male® are registered emblems with the Johns Hopkins College. Copyright® 1966-2024 Johns Hopkins College. Printed: Sept. 15, 2024 ×
essential Be aware: NIH isn't going to independently verify info submitted to your GTR; it relies on submitters to offer info that's correct and not misleading.
with specific questions on a genetic exam need to contact a wellness treatment supplier or even a genetics professional.
See apply and scientific guidelines in PubMed. The search results could include things like broader subjects and may not seize all printed tips. See the FAQ for facts.
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A seizure is really an intermittent abnormality of nervous process physiology characterized by a transient incidence of signs and/or indicators as a consequence of abnormal extreme or synchronous neuronal activity within the brain.
A delay inside the achievement of motor or mental milestones inside the domains of progress of a kid, such as motor abilities, speech and language, cognitive techniques, and social and psychological capabilities. This phrase must only be applied to describe small children young than 5 years of age.
Electroclinical attributes and phenotypic variances in adenylosuccinate lyase deficiency: prolonged-time period adhere to-up of 7 clients from 4 people and appraisal in the literature.
Fenfluramine provides clinically significant reduction in frequency of drop seizures in sufferers with Lennox-Gastaut syndrome: Interim Investigation of the open-label extension study.
carol : 07/21/2020 Be aware: OMIM is meant for use principally by physicians together with other professionals concerned with genetic Conditions, by genetics researchers, and by Innovative pupils in science and medication. While the OMIM database is open up to the public, customers trying to get details about a private health care or genetic issue are urged to consult with an experienced physician for prognosis and for answers to private issues. OMIM® and on-line Mendelian Inheritance in person® are registered trademarks of the Johns Hopkins University. Copyright® 1966-2024 Johns Hopkins College.
Fenfluramine provides clinically significant reduction in frequency of fall seizures in clients with Lennox-Gastaut syndrome: Interim Assessment of the open-label extension study.
Comparative security of antiepileptic medications for neurological advancement in small children uncovered during pregnancy and breast feeding: a scientific critique and community meta-Evaluation.
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OMIM Donation: expensive OMIM User, to be certain long-phrase funding with the OMIM job, We now have diversified our income stream. we've been established to maintain this Web-site freely available. sad to say, It's not at all free of charge to make. pro curators evaluate the literature and organize it to aid your do the job. about ninety% on the OMIM's running expenses head over to income aid for MD and PhD science writers and biocurators.
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