Wolcott-Rallison syndrome

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Monogenic Diabetes Misdiagnosed as Type 1	Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Deaf-Blind Disorders, Deafness, Ear Diseases, Eye Diseases, Hereditary, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Neurologic Manifestations, Nutritional and Metabolic Diseases, Sensation Disorders, Urogenital Diseases, Wolcott-Rallison syndrome, Wolfram syndrome, autoimmune disease, blindness (disorder), cranial nerve neuropathy, diabetes insipidus, diabetes mellitus, endocrine system disorder, eye disorder, glucose metabolism disease, hearing disorder, hearing loss disorder, hereditary disease, hereditary optic atrophy, immune system disorder, inherited neurodegenerative disorder, kidney disorder, maternally-inherited diabetes and deafness, metabolic disease, monogenic diabetes, nervous system disorder, neurodegenerative disease, optic atrophy, optic nerve disorder, otorhinolaryngologic disease, pituitary gland disorder, type 1 diabetes mellitus, urinary system disorder, vision disorder	Recruiting	Not stated	2024-12-10		NCT03988764

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