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Parry–Romberg syndrome

Parry–Romberg syndrome

Very Rare disease involving degeneration of tissues beneath the skin.

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Readers' pathsAug 2026 – Oct 2026

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Share of the 887 clicks on its links

  1. Morphea

    Form of scleroderma involving isolated patches of hardened skin.

    16%

  2. Hemifacial microsomia

    Birth defect which affects the lower half of the face.

    13%

  3. Caleb Hillier Parry

    Anglo-Welsh physician.

    7.3%

  4. Moritz Heinrich Romberg

    German physician (1795–1873).

    7.1%

  5. Goldenhar syndrome

    Rare birth defect; incomplete development of the face on one side.

    6.2%

  6. Scleroderma

    Group of autoimmune diseases resulting in abnormal growth of connective tissue.

    5.5%

  7. Trigeminal trophic syndrome

    Medical condition.

    5.3%

  8. Atrophy

    Partial or complete wasting away of a part of the body.

    2.4%

  9. Antinuclear antibody

    Autoantibody that binds to contents of the cell nucleus.

    1.4%

Readers come from

Share of the 529 readers arriving from another article

  1. Heterochromia

    Difference in coloration, usually of the iris but also of hair or skin.

    43%

  2. Oligoclonal band

    Marker in blood/cerebrospinal fluid testing.

    17%

  3. Caleb Hillier Parry

    Anglo-Welsh physician.

    5.9%

  4. Hemifacial microsomia

    Birth defect which affects the lower half of the face.

    4.9%

  5. Megalocornea

    Medical condition.

    4.3%

  6. Microtia

    Birth defect that affects the ears.

    2.1%