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10 Possible Causes for Alopecia, Cerebral Vasculitis or Vasculopathy, Gerstmann Syndrome

  • Stroke

    ), noninflammatory vasculopathy, Moyamoya disease and fibromuscular dysplasia.[en.wikipedia.org] MCA syndrome PCA syndrome frontal lobe : Expressive aphasia Aboulia parietal lobe : Receptive aphasia Hemispatial neglect Gerstmann syndrome Astereognosis occipital lobe[en.wikipedia.org] 10 643·5 to 22 842·6) 31·0 (29·7 to 32·4) * 5·1 (4·3 to 5·8) * 202·3 (136·5 to 292·9) 207·8 (140·1 to 300·1) 212·1 (143·0 to 306·4) 4·9 (4·2 to 5·6) * 2·1 (1·5 to 2·6) * Alopecia[ncbi.nlm.nih.gov]

  • ANE Syndrome

    vasculopathy or vasculitis. 4, 14, 15 In approximately 20% of children, the more severe form is encountered, with bilateral thalamic necrosis and restricted diffusion recently[ajnr.org] MCA syndrome PCA syndrome frontal lobe : Expressive aphasia Aboulia parietal lobe : Receptive aphasia Hemispatial neglect Gerstmann syndrome Astereognosis occipital lobe[en.wikipedia.org] Definition Affected individuals have hair loss of variable severity, ranging from complete alopecia to near-normal scalp hair with absence of body hair.[uniprot.org]

  • CANOMAD Syndrome

    Palato Cardiac Syndrome Genitopatellar Syndrome Genoa Syndrome German Syndrome Gerstmann syndrome Ghose Sachdev Kumar Syndrome Giacheti Syndrome Gilles de la Tourette syndrome[rgd.mcw.edu] […] venous thrombosis Laboratory Pathology: Vasculopathy Perivascular inflammation Systemic or CNS Association with: HLA-B51 CSF Abnormal in 75%: Especially with parenchymal[neuromuscular.wustl.edu] […] methylmalonic aciduriaCommon variable component Complement receptor canalComplex regional pain malformed earCone tapetallike sheenConerod amelogenesis Congenital absence adrenal alopecia[shecandothat.net]

  • Hypotrichosis - Lymphedema - Telangiectasia with Membranoproliferative Glomerulonephritis

    […] in the skin, liver and brain. [73] [74] No signs of cerebral vasculitis noted.[autoinflammatory-search.org] Syndrome Giant Axonal Neuropathy Gilbert Syndrome Gitelman Syndrome Glanzmann Thrombasthenia Glaucoma, Primary Congenital Glaucoma 1, Open Angle, E Glaucoma 1, Open Angle[sequencing.com] Alopecia universalis onychodystrophy vitiligo 0 *Alopecia *Nails, Malformed *Vitiligo. Alopecia universalis 0 *Alopecia.[reference.md]

  • Fetal Akinesia - Cerebral and Retinal Hemorrhage Syndrome

    • Malignancy and cerebral vasculitis• Drug-induced cerebral vasculitis 80.[slideshare.net] Combinations of finger agnosia, acalculia, right–left disorientation, and agraphia (Gerstmann’s syndrome) may be encountered.[neupsykey.com] […] partial loss of scalp hair Alopecia totalis: 100% loss of scalp hair Alopecia Universalis : 1oo% loss of hair on the scalp and body Ddx: Trichotillomania – patch with twisted[ccfpprep.com]

  • Progressive External Ophthalmoplegia - Myopathy - Emaciation Syndrome

    HMGB1 Testicular Germ Cell Tumor RFWD3 Thoracic Diseases ATRX Thrombosis SIRT1 Vacterl Association With Hydrocephalus FANCB Vasculopathy, Retinal, With Cerebral Leukodystrophy[selfdecode.com] Rett syndrome Orofaciodigital syndrome 2 Amelogenesis imperfecta Barth syndrome Gerstmann-Straussler-Scheinker disease Dysequilibrium syndrome Mohr-Tranebjaerg syndrome Shprintzen[checkrare.com] ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES Is also known as ane syndrome;alopecia-progressive neurological defect-endocrinopathy syndrome Related symptoms[mendelian.co]

  • Familial X-Linked Thrombocytosis

    […] in the skin, liver and brain. [73] [74] No signs of cerebral vasculitis noted.[autoinflammatory-search.org] ROBO3 Geroderma Osteodysplasticum GORAB Gerstmann-Straussler Disease PRNP Glaucoma, Primary Congenital CYP1B1 Glucose Transport Defect SLC2A1 Glucose-6-Phosphate Dehydrogenase[rgipgd.com] Other signs include skin lesions (eg, eczema, warts, abscesses, pyoderma, alopecia), oral or esophageal thrush, oral ulcers, and periodontitis.[merckmanuals.com]

  • Hereditary Arterial and Articular Multiple Calcification Syndrome

    […] in the skin, liver and brain. [73] [74] No signs of cerebral vasculitis noted.[autoinflammatory-search.org] Gerstmann syndrome a neurological disorder that includes a writing disability ( agraphia or dysgraphia ), a lack of understanding of the rules for calculation or arithmetic[strokecenter.org] Cruz-Rivera syndrome Mackay-Shek-Carr syndrome MACOM syndrome Macroblepharon-ectropion-hypertelorism-macrostomia syndrome Macrocephalic sperm head syndrome Macrocephaly-alopecia-cutis[orpha.net]

  • Cold-Induced Sweating Syndrome Type 2

    […] in the skin, liver and brain. [73] [74] No signs of cerebral vasculitis noted.[autoinflammatory-search.org] ., (Prion disease: Creutzfeldt-Jakob disease -CJD-, Gerstmann-Straussler-Scheinker syndrome and fatal familial insomnia -GSS- -FFI-) - Gen PRNP.[ivami.com] […] due to adenosine kinase deficiency Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase Hyperphosphatasia with mental retardation syndrome Hypogonadism, alopecia[qlinics.com]

  • Familial Acute Necrotizing Encephalopathy

    Primary small vessel cerebral vasculitis usually shows chronic or sub-acute asymmetrical neurological progression (2).[path.upmc.edu] […] with a cerebellar malformation as major feature Genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature Genitopatellar syndrome Gerstmann-Straussler-Scheinker[se-atlas.de] vasculitis and metabolic encephalopathy.[path.upmc.edu]

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