It is a complex progressive neurodegenerative condition which is very rare Wolfram syndrome type(WS2) (OMIM) is an autosomal recessive disorder caused by biallelic pathogenic variants in CISDLike classic WFS1 spectrum disorder (WFSSD), WS2 presents as a continuum of clinical features; however, the full clinical spectrum of WS2 abnormalities has not yet been fully established because so few affected Wolfram syndrome. Clinical and genetic heterogeneity, as well as Wolfram syndrome is a rare genetic disorder characterized by juvenile-onset diabetes mellitus, diabetes insipidus, optic nerve atrophy, hearing loss, and neurodegeneration Wolfram Syndrome is a genetic disorder that can cause a set of conditions which includes Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy and Deafness as well as several other conditions. Suggest an update. Disease definition. A rare, genetic, endocrine disorder characterized by type I diabetes mellitus (DM), diabetes insipidus (DI), sensorineural deafness (D), bilateral optical atrophy (OA) and neurological signs Wolfram syndrome (WS) is an autosomal recessive disorder characterized by diabetes insipidus (DI), childhood-onset diabetes mellitus (DM), a gradual loss of vision caused by optic atrophy (OA), deafness (D; hence the acronym: DI DM OA D), and neurological signs A rare, genetic, endocrine disorder characterized by type I diabetes mellitus (DM), diabetes insipidus (DI), Wolfram syndrome (OMIM) is a rare autosomal recessive disease with a devastating array of symptoms, including diabetes mellitus, optic nerve atrophy, Abstract: Wolfram Syndrome (WS) is an ultra-rare, progressive neurodegenerative disease characterized by early-onset diabetes mellitus and irreversible loss of vision, secondary Wolfram syndrome is a rare genetic disorder with more than pathogenic variants reported in association with disease. Disease definition. Suggest an update. Wolfram Syndrome is a genetic disorder that can cause a set of conditions which includes Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy and Deafness as well as several Wolfram syndrome.
It is a complex progressive neurodegenerative condition which is very rare Wolfram syndrome type(WS2) (OMIM) is an autosomal recessive disorder caused by biallelic pathogenic variants in CISDLike classic WFS1 spectrum disorder (WFSSD), WS2 presents as a continuum of clinical features; however, the full clinical spectrum of WS2 abnormalities has not yet been fully established because so few affected Wolfram syndrome. Clinical and genetic heterogeneity, as well as Wolfram syndrome is a rare genetic disorder characterized by juvenile-onset diabetes mellitus, diabetes insipidus, optic nerve atrophy, hearing loss, and neurodegeneration Wolfram Syndrome is a genetic disorder that can cause a set of conditions which includes Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy and Deafness as well as several other conditions. Suggest an update. Disease definition. A rare, genetic, endocrine disorder characterized by type I diabetes mellitus (DM), diabetes insipidus (DI), sensorineural deafness (D), bilateral optical atrophy (OA) and neurological signs Wolfram syndrome (WS) is an autosomal recessive disorder characterized by diabetes insipidus (DI), childhood-onset diabetes mellitus (DM), a gradual loss of vision caused by optic atrophy (OA), deafness (D; hence the acronym: DI DM OA D), and neurological signs A rare, genetic, endocrine disorder characterized by type I diabetes mellitus (DM), diabetes insipidus (DI), Wolfram syndrome (OMIM) is a rare autosomal recessive disease with a devastating array of symptoms, including diabetes mellitus, optic nerve atrophy, Abstract: Wolfram Syndrome (WS) is an ultra-rare, progressive neurodegenerative disease characterized by early-onset diabetes mellitus and irreversible loss of vision, secondary Wolfram syndrome is a rare genetic disorder with more than pathogenic variants reported in association with disease. Disease definition. Suggest an update. Wolfram Syndrome is a genetic disorder that can cause a set of conditions which includes Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy and Deafness as well as several Wolfram syndrome.
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