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54 Possible Causes for Beaked Nose, Calcinosis, Systemic Scleroderma

  • Systemic Scleroderma

    We describe 2 patients with systemic sclerosis who have multiple umbilicated nodules indistinguishable from calcinosis cutis.[ncbi.nlm.nih.gov] Face Matt telangiectases on face, chest, palms Peri-oral furrowing (fat loss) Microstomia (limited oral aperture defined as interlabial distance 4.5 cm) Beaked nose Other[dermnetnz.org] Patients diagnosed with systemic scleroderma can be categorized under two wide categories: diffuse systemic sclerosis (dSSc) and limited cutaneous systemic sclerosis (lSSc[symptoma.com]

  • Diffuse Scleroderma

    In contrast to SSc, Raynaud's phenomenon and cutaneous calcinosis were absent and antinuclear antibodies were negative.[ncbi.nlm.nih.gov] Face Matt telangiectases on face, chest, palms Peri-oral furrowing (fat loss) Microstomia (limited oral aperture defined as interlabial distance 4.5 cm) Beaked nose Other[dermnetnz.org] […] sclerosis or systemic scleroderma Progressive systemic sclerosis Scleroderma syndrome Scleroderma PSS Systemic Scleroderma Scleroderma, Diffuse SSc Scleroderma, Systemic[wikidata.org]

  • Limited Cutaneous Systemic Sclerosis

    Abstract We describe a patient with a 23-year history of progressive calcinosis and features of the CREST syndrome (calcinosis, Raynaud's phenomenon, esophageal dysmotility[ncbi.nlm.nih.gov] […] like nose -Shiny skin -Taut lips -Salt and pepper hypo/hyperpigmentation Sclerodactyly in systemic scleroderma -The skin is very taut -Painful -Easy to get digital ulcers[quizlet.com] Scleroderma renal crisis in a patient with anticentromere antibody-positive limited cutaneous systemic sclerosis. Mod Rheumatol 2006;16(5):309-11. 61.[degruyter.com]

  • Sclerodactyly

    Abstract A 58-year-old woman with calcinosis Raynaud esophageal sclerodactyly telangiectasia (CREST) syndrome presented with slowly progressive renal dysfunction.[ncbi.nlm.nih.gov] Systemic scleroderma often affects the hands. The initial stage is swelling (edema), which can last for weeks, months, or years.[doctorsgates.blogspot.com] Face Matt telangiectases on face, chest, palms Peri-oral furrowing (fat loss) Microstomia (limited oral aperture defined as interlabial distance 4.5 cm) Beaked nose Other[dermnetnz.org]

  • Scleroderma

    RESULTS: There were 215 SSc patients, including 65 SSc-calcinosis (81.5% females) and 150 SSc-without calcinosis (controls, 77% females).[ncbi.nlm.nih.gov] systemic scleroderma .[ghr.nlm.nih.gov] Face Matt telangiectases on face, chest, palms Peri-oral furrowing (fat loss) Microstomia (limited oral aperture defined as interlabial distance 4.5 cm) Beaked nose Other[dermnetnz.org]

  • Werner Syndrome

    Here we report a 29-year-old female patient who displayed cataracts, hair graying, and tendinous calcinosis. Her parents were first cousins.[ncbi.nlm.nih.gov] An excellent discussion of the distinguishing features that separate systemic scleroderma from WS is also presented.) Capell, BC, Tlougan, BE, Orlow, SJ.[dermatologyadvisor.com] Grating hair, scanty eyebrows, a pinched or beaked nose, protuberant eyes and the absence of eyelashes contribute to the presenile appearance.[whonamedit.com]

  • Progeria

    Marked skin calcinosis was observed over almost the entire body, a symptom that has apparently been ignored in the literature.[ncbi.nlm.nih.gov] […] wasting, skin atrophy, disseminated skeletal osteoporosis (documented for at least 25 years), especially in the vertebral column and metacarpal joints with short stature, beaked[ncbi.nlm.nih.gov] The child also presented scleroderma plaques on the abdomen.[ncbi.nlm.nih.gov]

  • Nestor-Guillermo Progeria Syndrome

    […] cataracts (requiring surgery at a median age of 30); hypertension, premature and severe forms of arteriosclerosis (including atherosclerosis, arteriolosclerosis and medial calcinosis[karger.com] […] blood vessels, muscles, and internal organs.There are two main types: localized scleroderma, which affects only the skin; and systemic scleroderma, which affects the blood[checkrare.com] Waardenburg syndrome (WS) Adiponectin deficiency Enterokinase deficiency Diseases of the tricarboxylic acid cycle CD36 deficiency Sea-blue histiocyte disease Familial tumoral calcinosis[csirnotes.com]

  • Crouzon Syndrome-Acanthosis Nigricans Syndrome

    […] deficiency Monomelic amyotrophy Pycnodysostosis Autosomal dominant hypophosphatemic rickets Deafness with labyrinthine aplasia, microtia, and microdontia Hypercalcemic tumoral calcinosis[csbg.cnb.csic.es] The craniosynostosis causes changes to the shape of the head as well as unique facial features that may include wide-set eyes, a beaked nose, and a small upper jaw.[diseaseinfosearch.org] We report on an infant who presented at birth with multisuture synostosis, turribrachycephaly, midface hypoplasia, beaked nose, low set ears, a high palate and short squat[onlinelibrary.wiley.com]

  • Familial Scaphocephaly Syndrome

    […] with amyloidosis, Piedmont type Aldosterone-producing adenoma with seizures and neurological abnormalities Autosomal dominant hypophosphatemic rickets Hypercalcemic tumoral calcinosis[csbg.cnb.csic.es] Affected individuals have distinct facial featurs like bulging ees, beaked nose, and underdeveloped jaws. Apert syndrome is similar to Crouzon syndrome.[abcore.com] Affected individuals have distinct facial features like bulging eyes, a beaked nose, and underdeveloped jaws. Apert syndrome is similar to Crouzon syndrome.[abcore.com]

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