Hyperglycemic Hyperosmolar State as the Initial Presentation of Wolfram Syndrome: A Common Complication Revealing a Rare Disease—A Case Report [PDF]
Wolfram syndrome is a rare autosomal recessive disorder characterized by diabetes insipidus, diabetes mellitus, optic atrophy, and deafness (DIDMOAD).
Sushrut Ingawale +4 more
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A Rare Case of Wolfram Syndrome Presenting With Tuberculous Meningitis: A Case Report [PDF]
Wolfram syndrome is an extremely rare condition composed of a tetrad of diabetes insipidus, diabetes mellitus, optic atrophy, and deafness. When concurrently presenting with another condition, such as tuberculous meningitis, the widespread range of ...
Nabiha Khan +6 more
doaj +3 more sources
Case Report: Rapid cataract development preceding diabetes mellitus in WFS1 spectrum disorder [PDF]
WFS1 spectrum disorder is a rare condition, characterized by diabetes insipidus, diabetes mellitus, optic atrophy, and deafness (DIDMOAD). A 2-year-old female patient with a history of sensorineural hearing loss presented with rapid, sequential cataract ...
Aaishwariya A. Gulani +6 more
doaj +4 more sources
The Presence of Periodic Limb Movement Disorder in a Patient with Diabetes Mellitus and Optic Atrophy (Wolfram Syndrome) [PDF]
Wolfram syndrome (WFS) is characterized by diabetes insipidus, diabetes mellitus, optic atrophy, and deafness (DIDMOAD), together known as DIDMOAD. This syndrome is a rare autosomal recessive neurodegenerative disorder and typically begins wtih insulin ...
Bo Seong Kwon, Su-Hyun Han, Sang-Ahm Lee
doaj +2 more sources
Sluchay netipichnogo techeniya DIDMOAD-sindroma
Один из наиболее изученных и распространенных генетических синдромов, включающих в себя СД 1 ? DlDMOAD-синдром. Развитие DIDMOAD-синдрома обусловлено митохондриальной дисфункцией.
Tamara Leonidovna Kuraeva +1 more
doaj +2 more sources
Wolfram syndrome: Portuguese research [PDF]
INTRODUCTION: Wolfram syndrome (WFS) is a neurological and endocrinological degenerative disorder, also known as DIDMOAD (Diabetes Insipidus, early-onset Diabetes Mellitus, progressive Optic Atrophy, and Deafness) syndrome.
Cristina Ferreras +6 more
doaj +2 more sources
Novel Presentation of Type 1 Wolfram Syndrome as Intracranial Hemorrhage and Longitudinally Extensive Transverse Myelitis: Neuroimaging and Angiographic Findings [PDF]
Wolfram syndrome (WS), a rare genetic neurodegenerative condition, is primarily characterized by diabetes mellitus, optic atrophy, diabetes insipidus, and sensorineural hearing loss, along with diverse systemic manifestations.
Ravi P Singh +5 more
doaj +2 more sources
Diabetes mellitus, diabetes insipidus, optic atrophy and deafness (DIDMOAD syndrome)
Two patients with diabetes mellitus (DM), diabetes insipidus (DI), optic atrophy (OA), deafness (D) and dilatation of the urinary tract-the so-called DIDMOAD syndrome are presented. In one of the patients, the presenting components were DI and OA.
U Saatçi +4 more
doaj +5 more sources
Various clinical aspects of DIDMOAD (Wolfram) syndrome
The association of juvenile diabetes mellitus (DM), diabetes insipidus (DI), optic atrophy (OA) and sensorineural deafness (D) is known as DIDMOAD or Wolfram syndrome. Aside from these four cardinal features, a wide variety of abnormalities of the
A Okten +5 more
doaj +3 more sources
Gonadal Dysfunction in Wolfram Syndrome: A Prospective Study [PDF]
Background: Wolfram syndrome (WFS), also known as DIDMOAD, is a rare monogenic neurodegenerative disorder characterized by four key components: non-autoimmune insulin-dependent diabetes mellitus (DM), optic atrophy, sensorineural hearing loss, and ...
Gema Esteban-Bueno +1 more
doaj +2 more sources

