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7,052 Possible Causes for Onset in Infancy

Did you mean: Onset in, Infancy

  • Wolcott-Rallison Syndrome

    We present the case of a 13-year-old Greek boy with a known history of infancy-onset diabetes mellitus and was found to have WRS at the age of 4 years.[ncbi.nlm.nih.gov] In 1972, Wolcott and Rallison described three siblings with a combination of infancy-onset diabetes mellitus and multiple epiphyseal dysplasia.[ncbi.nlm.nih.gov] The clinical phenotype associated with the syndrome can be variable, but a combination of infancy-onset diabetes mellitus, multiple epiphyseal dysplasia, and hepatic and/or[ncbi.nlm.nih.gov]

  • Early Infantile Epileptic Encephalopathy Type 6

    […] in infancy with polymorphous seizure types and developmental decline.[ncbi.nlm.nih.gov] Target population includes those with electroclinical phenotype of Dravet Syndrome or clinical sub-types – several seizure types in one individual with onset in infancy, refractory[currents.plos.org] Onset in first year of life Onset in infancy About 10-20% of people with this condition are estimated to pass away before adulthood, with most premature deaths occurring[rarediseases.info.nih.gov]

  • Transient Hypogammaglobulinemia of Infancy

    Abstract Tansient hypogammaglobulinemia of infancy (THI) is characterized by an abnormal delay in the onset of immunoglobulin synthesis.[ncbi.nlm.nih.gov] Introduction Transient hypogammaglobulinemia of infancy (THI) is the delayed onset of normal immunoglobulins level, usually IgG Pathophysiology normal physiology maternal[medbullets.com] Transient hypogammaglobulinemia of infancy (disorder) THI edit English transient hypogammaglobulinemia of infancy form of hypogammaglobulinemia appearing after birth, leading[wikidata.org]

  • Familial Infantile Myoclonic Epilepsy

    ORPHA:352582 Synonym(s): FIME Familial infantile myoclonus epilepsy Prevalence: Inheritance: Autosomal recessive Age of onset: Infancy, Neonatal ICD-10: G40.3 OMIM: 605021[orpha.net] Myoclonic epilepsies with onset in infancy and childhood are clinically and etiologically heterogeneous but, as a group, may be refractory to treatment.[emedicine.medscape.com] Mutations in this gene cause NCL with a wide clinical spectrum - typical onset is in infancy but can be delayed until adulthood.[ucl.ac.uk]

  • Overeating

    Book Info for When Women Stop Hating Their Bodies Kids, Carrots, and Candy Book Information Description In this comprehensive parent-child guide to eating behaviors (from infancy[overcomingovereating.com] Eating to Ease Stress From infancy on, eating is soothing. Emotional stress plays perhaps the best-known role in the urge to overeat.[theatlantic.com]

  • Generalized Epilepsy with Febrile Seizures Plus

    […] epilepsy in infancy (SMEI) were 9, 11, 7, and 7, respectively.[ncbi.nlm.nih.gov] The cases described here are of two brothers, one with severe myoclonic epilepsy of infancy (Dravet syndrome) and the other myoclonic-astatic epilepsy.[ncbi.nlm.nih.gov] Refractory grand mal seizures with onset during infancy including severe myoclonic epilepsy in infancy.[jcomjournal.com]

  • West Syndrome

    The current spectrum of disorders associated to clinical spasms with onset in infancy is wider than previously thought; accordingly, its terminology has changed.[ncbi.nlm.nih.gov] - A dictionary of medical eponyms Related people William James West A form of myoclonus epilepsy with onset in infancy or early childhood.[whonamedit.com] Abstract The West syndrome and the Lennox-Gas-taut syndrome are characterized by their onset in infancy and early childhood, intractable seizures occurring almost daily, severe[pediatrics.aappublications.org]

  • Myoclonic-Astatic Epilepsy

    Severe myoclonic epilepsy of infancy (Dravet syndrome) Severe myoclonic epilepsy of infancy (SMEI) is an uncommon disorder with onset between 3 months and 2 years of age.[emedicine.medscape.com] Myoclonic epilepsies with onset in infancy and childhood are clinically and etiologically heterogeneous but, as a group, may be refractory to treatment.[emedicine.medscape.com] Abstract Severe myoclonic epilepsy in infancy (SMEI), severe idiopathic generalized epilepsy of infancy (SIGEI) with generalized tonic clonic seizures (GTCS), and myoclonic[ncbi.nlm.nih.gov]

  • Neonatal Adrenoleukodystrophy

    Clinical description NALD has an onset at birth or early infancy, but manifestations may be subtle enough that it is not diagnosed until late infancy or early childhood (or[orpha.net] Prognosis Prognosis is poor with most patients dying in infancy and early childhood. Some have lived until their teenage years. Last updated: 12/1/2012[rarediseases.info.nih.gov] Cataracts should be removed in early infancy and glasses used to improve vision.[orpha.net]

  • Infantile Hepatic Hemangioendothelioma

    Hepatic hemangioendotheliomas in infancy. Surg Gynecol Obstet 1989;168:189–200. 13. Selby DM, Stocker JT, Waclawiw MA, Hitchcock CL, Ishak KG.[synapse.koreamed.org] Abstract Infantile hepatic hemangioendothelioma is a rare tumor of infancy, sometimes associated with cutaneous hemangiomatosis.[link.springer.com] Infantile hepatic hemangioendothelioma is a rare tumor of infancy, sometimes associated with cutaneous hemangiomatosis.[ncbi.nlm.nih.gov]

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