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1,446 Possible Causes for Juvenile Familial Leg Ulcers, Progeria

  • Werner Syndrome

    Neuropathy or familial leg ulcers of juvenile onset.[] Progeria, also known as Hutchinson-Gilford progeria syndrome (HGPS), is a rare genetic condition that causes a child's body to age fast.[] Hutchinson-Gilford progeria syndrome most closely resembles WS.[]

  • Cardiomyopathy

    Cardiomyopathy is disease in which the heart muscle becomes weakened, stretched, or has another structural problem. It often occurs when the heart cannot pump or function well. Most people with cardiomyopathy have heart failure. There are many types of cardiomyopathy, with different causes. Some of the more[…][]

    Missing: Juvenile Familial Leg Ulcers
  • Cockayne Syndrome

    […] photosensitivity, progressive neurological dysfunction, and intellectual deficit Neill-Dingwall syndrome, Kenny Syndrome Neill-Dingwall syndrome Cockayne's syndrome Hutchinson–Gilford progeria[] Cockayne syndrome is a kind of progeria with autosomal chromosome recessiveness described first by Cockayne in 1936.[] She had displayed the striking features of CS, including dwarfism, mental retardation, neural deafness, ataxia, intracranial calcifications, and progeria since her childhood[]

    Missing: Juvenile Familial Leg Ulcers
  • Progeria

    […] the word «progeria».[] All these tests confirm the diagnosis of progeria. So far, no breakthrough has been made for treating progeria. Progeria has no cure.[] As newborns, children with progeria usually appear normal.[]

    Missing: Juvenile Familial Leg Ulcers
  • Nestor-Guillermo Progeria Syndrome

    We describe herein the clinical features of the first two NGPS patients, who phenocopy features of classic progerias (i.e., Hutchinson-Gilford progeria syndrome or mandibuloacral[] Names and Terminology for Nestor-guillermo progeria syndrome Other Names : NGPS; Progeria syndrome , childhood-onset , with osteolysis ; PSCOO Source: GARD (NIH) 1 • • • PROGERIA[] Entry H01883 Disease Name Nestor-Guillermo progeria syndrome Description Nestor-Guillermo progeria syndrome (NGPS) is a new hereditary progeroid syndrome.[]

    Missing: Juvenile Familial Leg Ulcers
  • Wiedemann-Rautenstrauch Syndrome

    L.: The Hutchinson-Gilford progeria syndrome. J. of Pediatr. 80, 697 (1972) Google Scholar Djupesland, T.: Progeria.[] DeBusk FL (1972) The Hutchinson-Gilford progeria syndrome. J Pediatr 80:697–724 Google Scholar 2.[] DeBusk FL (1972) The Hutchinson-Gilford progeria syndrome. J Pediatr 80:697–724 Google Scholar 6.[]

    Missing: Juvenile Familial Leg Ulcers
  • Acroosteolysis-Keloid-Like Lesions-Premature Aging Syndrome

    Stem cell aging in adult progeria. Cell Regeneration, 4, 1–9. CrossRef Google Scholar Cooke, J. V. (1953). The rate of growth in progeria.[] Cooke JV: The rate of growth in progeria. J Pediatr 42:26–37, 1953 CrossRef PubMed Google Scholar 11. Danes BS: Progeria: a cell culture study on aging.[] Progeria. Arch Dermatol 1989;125:540544.7. Hamer L, Kaplan F, Fallon M. The musculoskeletal mani-festations of progeria: a literature review.[]

    Missing: Juvenile Familial Leg Ulcers
  • Micrognathism

    It also causes unusually short: legs arms neck torso Progeria Progeria is a genetic condition that causes your child to age at a rapid rate.[] […] part of Goldenhar syndrome) Incontinentia pigmenti Juvenile idiopathic arthritis Marfan syndrome Möbius syndrome Noonan syndrome Pierre Robin syndrome Prader–Willi syndrome Progeria[] […] dimension and contour of the ridge following tooth… (More) Shao Hai Yang, Margarita Meta, 7 authors Loren G Fong The Journal of clinical investigation 2006 Hutchinson-Gilford progeria[]

    Missing: Juvenile Familial Leg Ulcers
  • Acroosteolysis

    PINCHFO.Pyknodysostosis, Psoriasis, Injury (thermal burn, frostbite), Neuropathy (diabetes), Collagen vascular disease (scleroderma, Raynaud's), Hyperparathyroidism, Familial (Hadju-Cheney, progeria[] […] however, patients lack premature aging seen in progeria and increased bone density and decreased mandible angle observed in pycnodysostosis.[] Differential diagnosis Differential diagnoses may include pycnodysostosis and Hutchinson-Gilford progeria syndrome (see these terms) based on clinical and x-ray findings,[]

    Missing: Juvenile Familial Leg Ulcers
  • Congenital Muscular Dystrophy due to LMNA Mutation

    […] right dominant form Familial partial lipodystrophy, Dunnigan type Familial partial lipodystrophy, Köbberling type Heart-hand syndrome, Slovenian type Hutchinson-Gilford progeria[] Hutchinson-Gilford progeria 176670 Malouf syndrome 212112 Heart-hand syndrome, Slovenian type 610140 Mandibuloacral dysplasia 248370[] Denecke J, Wasner C, Feuer A, Marquardt T, Ketelsen UP, Wieacker P, Bonnemann CG, Korinthenberg R Title p.S143F mutation in lamin A/C: a new phenotype combining myopathy and progeria[]

    Missing: Juvenile Familial Leg Ulcers

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