Skin crease extending from underneath the inner canthus laterally alongside the malar strategy of the maxilla and zygoma.
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HelpList of clinical characteristics of your affliction/phenotype exhibited from resources like the Human Phenotype Ontology (HPO) and OMIM. To learn more in regards to the condition, make sure you go to the condition facts web site.
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A seizure is an intermittent abnormality of anxious process physiology characterized by a transient event of indications and/or signs resulting from abnormal too much or synchronous neuronal exercise within the Mind.
Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing.
Electroclinical functions and phenotypic dissimilarities in adenylosuccinate lyase deficiency: Long-phrase comply with-up of 7 patients from 4 people and appraisal from the literature.
prolonged-time period developmental consequence of kids of girls with epilepsy, unexposed or uncovered prenatally to antiepileptic prescription drugs: a meta-Examination of cohort reports.
carol : 07/21/2020 Take note: OMIM is intended to be used largely by doctors and various experts worried about genetic Problems, by genetics researchers, and by advanced pupils in science and click here medication. While the OMIM database is open up to the public, end users trying to find details about a personal health care or genetic ailment are urged to consult with an experienced health practitioner for diagnosis and for solutions to non-public queries. OMIM® and on-line Mendelian Inheritance in person® are registered trademarks with the Johns Hopkins University. Copyright® 1966-2024 Johns Hopkins College.
NIH makes no endorsements of assessments or laboratories outlined during the GTR. GTR will not be a substitute for healthcare information. Patients and individuals
Comparative protection of antiepileptic medication for neurological growth in children uncovered throughout pregnancy and breast feeding: a scientific evaluate and community meta-Investigation.
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