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101 Possible Causes for Alopecia, Beaked Nose, Systemic Scleroderma

  • Werner Syndrome

    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] Werner syndrome (WS), such as high-pitched voice, scleroderma, lipoatrophy and atherosclerosis, several cardinal features of WS, including short stature, premature graying/alopecia[ncbi.nlm.nih.gov]

  • Hallermann-Streiff Syndrome

    […] sclerosis, Skerodermie ICD 10: M34.0 Synonyme: Progressive systemic sclerosis, Scleroderma, CREST syndrome Spinale Muskelatrophie ( 1 Files ) Erkrankung: Spinale Muskelatrophie[orphananesthesia.eu] The Hallermann-Streiff syndrome is characterized by bird-like face, micropthalmia, cataracts, micrognathia, beaked nose, abnormal dentition, hypotrichosis, cutaneous atrophy[ncbi.nlm.nih.gov] […] overlying skull sutures, or alopecia areata and hypoplasia, or absence of eyebrows.[biology-online.org]

  • Diffuse Scleroderma

    Scleroderma Diffuse Systemic Scleroderma is a type of Systemic Scleroderma of unknown cause.[dovemed.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] Her past medical history includes autoimmune thyroid disease and alopecia areata.[medbullets.com]

  • Progeria

    The child also presented scleroderma plaques on the abdomen.[ncbi.nlm.nih.gov] The children usually present in late infancy and early childhood with a characteristic phenotype of alopecia; short stature; abnormal skin, teeth, and nails; beaked nose;[ncbi.nlm.nih.gov] At 18 months of age, irregular pigmentary changes of the abdomen, early occipital alopecia, superficial scalp veins, glyphic nasal tip, absent ear lobules, coarse hair that[ncbi.nlm.nih.gov]

  • Sclerodactyly

    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] The main manifestations are total congenital alopecia, bilateral congenital cataracts, and skin changes of the hands and feet including sclerodactyly, hyperkeratosis, contractures[ncbi.nlm.nih.gov]

  • Bangstad Syndrome

    Examples of common systemic autoimmune diseases include rheumatoid arthritis , systemic lupus erythematosus, diabetes mellitus, Sjogren syndrome, scleroderma , Goodpasture[medicinenet.com] The most common symptoms of this syndrome would be short stature, goiter, diabetes, ataxia, deafness, small head, mental retardation, beaked nose, clubfoot, undescended testes[symptoms.in] Particularly disheartening in this illness may be the occurrence of alopecia.[omicsonline.org]

  • Systemic Scleroderma

    […] sclerosis or systemic scleroderma Progressive systemic sclerosis Scleroderma syndrome Scleroderma PSS Systemic Scleroderma Scleroderma, Diffuse SSc Scleroderma, Systemic[wikidata.org] 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] Systemic scleroderma cannot be prevented.[symptoma.com]

  • Sanjad-Sakati Syndrome

    DISCUSSION Intestinal pseudo obstruction encompasses a broad range of disorders and is classified as primary (idiopathic) or secondary to other diseases (scleroderma, systemic[ghrnet.org] The facial features included microcephaly, thin lips, beaked nose, low set ears, and a retrognathic mandible.[ncbi.nlm.nih.gov] Synonym(s): Sakati-Nyhan syndrome Sakati-Nyhan syndrome - rare syndrome, usually sporadic, featuring craniofacial defects, abnormal limbs, congenital heart defects, patchy alopecia[medical-dictionary.thefreedictionary.com]

  • Nestor-Guillermo Progeria Syndrome

    […] 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] B: Typical facial features of HGPS (alopecia, beaked nose, micrognathia) and leucomelanodermic lesions in neck. C. Dystrophic nails.[tandfonline.com] They are characterized by features of normal aging such as alopecia, skin wrinkling, osteoporosis, insulin resistance, and cardiovascular disease.[genome.jp]

  • Acroosteolysis-Keloid-Like Lesions-Premature Aging Syndrome

    JDMS MCTD Undifferentiated connective tissue Scleroderma-like disorders : GVHD, nephrogenic systemic fibrosis, chemically induced scleroderma How does GVHD resemble scleroderma[quizlet.com] Her face wassmall, with a recessed chin, thin beaked nose, and smallears without earlobes, giving the face a birdlike appear-ance (Fig. 1).[documents.tips] LeRoy, EC; Black, C; Fleischmajer, R; et al. , Scleroderma (systemic sclerosis): classification, subsets and pathogenesis , J Rheumatol 15 ( 1988 ) 202 – 205 . 21.[plasticsurgerykey.com]

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