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  2. Autosomal dominant multiple pterygium syndrome - Wikipedia

    en.wikipedia.org/wiki/Autosomal_dominant...

    Autosomal dominant multiple pterygium syndrome is a cutaneous condition inherited in an autosomal dominant fashion. [2] Society

  3. Popliteal pterygium syndrome - Wikipedia

    en.wikipedia.org/wiki/Popliteal_pterygium_syndrome

    Bartsocas-Papas syndrome is a form of popliteal pterygium syndrome and is a very rare disease characterized by congenital craniofacial anomalies, popliteal webbing, and genitourinary and musculoskeletal anomalies. It was first described by Dr. Christos Bartsocas and is more specifically an autosomal recessive popliteal pterygium syndrome. [8]

  4. Pterygium (eye) - Wikipedia

    en.wikipedia.org/wiki/Pterygium_(eye)

    Symptoms of pterygium include persistent redness, [9] inflammation, [10] foreign body sensation, tearing, dry and itchy eyes. In advanced cases the pterygium can affect vision [ 10 ] as it invades the cornea with the potential of obscuring the optical center of the cornea and inducing astigmatism and corneal scarring. [ 11 ]

  5. List of skin conditions - Wikipedia

    en.wikipedia.org/wiki/List_of_skin_conditions

    Mitochondrial myopathy–encephalopathy–lactic acidosis–stroke syndrome; Multiple lentigines syndrome (cardiocutaneous syndrome, Gorlin syndrome II, lentiginosis profusa syndrome, LEOPARD syndrome, progressive cardiomyopathic lentiginosis) Multiple pterygium syndrome; Multiple sulfatase deficiency (Austin disease, mucosulfatidosis)

  6. Ankyloblepharon - Wikipedia

    en.wikipedia.org/wiki/Ankyloblepharon

    Popliteal pterygium syndrome (PPS): Popliteal pterygium syndrome (PPS) is a rare autosomal dominant disorder, first described by Trelat in 1869. The clinical features of the syndrome are highly variable and show different combinations of anomalies like cleft palate, cleft lip, lower lip pits or sinuses, popliteal webbing, syndactyly ...

  7. Autoimmune polyendocrine syndrome type 1 - Wikipedia

    en.wikipedia.org/wiki/Autoimmune_polyendocrine...

    Autoimmune polyglandular syndrome type 1, Whitaker syndrome, Candidiasis-hypoparathyroidism–Addison's disease syndrome: Autoimmune polyendocrine syndrome type 1 is autosomal recessive: Specialty: Endocrinology, medical genetics: Symptoms: chronic mucocutaneous candidiasis: Causes: mutation in AIRE gene: Diagnostic method: CT scan, biopsy ...

  8. Signs and symptoms of multiple sclerosis - Wikipedia

    en.wikipedia.org/wiki/Signs_and_symptoms_of...

    Treatments can be classified in two main subtypes: pharmacological and non-pharmacological. Pharmacological treatments vary greatly depending on the origin or type of dysfunction and some examples of the medications used are: [55] alfuzosin for retention, [56] trospium and flavoxate for urgency and incontinency, [57] [58] and desmopressin for ...

  9. Pterygium inversum unguis - Wikipedia

    en.wikipedia.org/wiki/Pterygium_inversum_unguis

    Pterygium inversum unguis or ventral pterygium is characterized by the adherence of the distal portion of the nailbed to the ventral surface of the nail plate. [ 3 ] : 788 The condition may be present at birth or acquired, and may cause pain with manipulation of small objects, typing, and close manicuring of the nail.