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109 Possible Causes for Onset in Infancy - First Year of Life

  • Autosomal Recessive Deafness 103

    الصفحة 296 - Embryonic stem cells develop into functional dopaminergic neurons after transplantation in a Parkinson rat model. ‏ الصفحة 108 - Mutation in mitochondrial tRNAIeu (UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nat. Genet. ‏ الصفحة 312 - Lumelsky, N.,[…][books.google.com]

  • Streptococcal Infection

    About 12,000 of the 3.5 million babies born in the United States each year develop GBS disease in infancy. About 75% of them develop early-onset infection.[medical-dictionary.thefreedictionary.com] Sometimes evident within a few hours of birth and always apparent within the first week of life, this condition causes inflammation of the membranes covering the brain and[medical-dictionary.thefreedictionary.com]

  • Atopic Dermatitis

    What you should be alert for in the history Onset occurs in the first year of life in approximately 60% of patients, with most developing signs and symptoms between the third[clinicaladvisor.com] Atopic dermatitis (AD) is a chronic, relapsing, pruritic dermatosis that commonly presents in early infancy or childhood.[clinicaladvisor.com]

  • Familial Infantile Myoclonic Epilepsy

    3 years of life ( Dravet and Bureau 1981 ).[medlink.com] Historical note and terminology Dravet and Bureau in 1981 described “benign myoclonic epilepsy in infancy” in 7 normal children with onset of myoclonic seizures in the first[medlink.com]

  • Generalized Epilepsy with Febrile Seizures Plus

    SCN1A mutations occur also in severe myoclonic epilepsy of infancy (SMEI), a rare convulsive disorder characterized by febrile seizures with onset during the first year of[doi.org] […] by febrile seizures with onset during the first year of life, followed by intractable epilepsy, impaired psychomotor development, and ataxia ( Dravet and Bureau, 1981 ; Scheffer[doi.org] life, followed by intractable epilepsy, impaired psychomotor development, and ataxia ( 12, 13 ).[doi.org]

  • Benign Familial Infantile Epilepsy

    6 years of life are benign myoclonic epilepsy of infancy.[emedicine.medscape.com] Age of onset is usually between 4 months and 3 years. [6] However, as reported by Rossi et al, later onset up to 4 years and 8 months is possible. [7] Genetics The genetics[emedicine.medscape.com] Dravet and Bureau found that the syndrome occurs in 7% of children with myoclonus and in 2% of epileptic children aged 1-36 months; 0.39 of epilepsies that begin in the first[emedicine.medscape.com]

  • West Syndrome

    West syndrome: Infantile spasms, a seizure disorder of infancy and early childhood with the onset predominantly in the first year of life of myoclonic seizures, hypsarrhythmia[medicinenet.com]

  • Osteomyelitis

    About 12, 000 of the 3.5 million babies born in the United States each year develop GBS disease in infancy. About 75% of them develop early-onset infection.[web.archive.org] Sometimes evident within a few hours of birth and always apparent within the first week of life, this condition causes inflammation of the membranes covering the brain and[web.archive.org]

  • Kostmann Syndrome

    Onset in first year of life Onset in infancy [ more ] 0003593 Monocytosis High blood monocyte number 0012311 Neutropenia Low blood neutrophil count Low neutrophil count [[rarediseases.info.nih.gov] 0005541 Eosinophilia High blood eosinophil count 0001880 Growth abnormality Abnormal growth Growth issue [ more ] 0001507 Increased antibody level in blood 0010702 Infantile onset[rarediseases.info.nih.gov]

  • Dravet Syndrome

    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] “Severe myoclonic epilepsy in infancy” was first described in 1978 by Charlotte Dravet, who observed common features: onset in the first year of life, fever sensitivity, multiple[ilae.org] Key points • Dravet syndrome is 1 of the most severe epilepsies in infancy. • The onset is always in the first year of life in apparently normal infants. • It is genetically[medlink.com]

Further symptoms