hypertrichosis lanuginosa(redirected from Ambras syndrome)
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hypertrichosis lanugino´sa persistent or acquired production of lanugo. It may be a congenital, autosomal dominant disorder in which there is excessive hair distributed over the entire body throughout life, usually in association with other congenital anomalies; or it may be acquired, with the degree of hairiness being variable, usually involving the face, and in most cases associated with internal carcinoma.
Miller-Keane Encyclopedia and Dictionary of Medicine, Nursing, and Allied Health, Seventh Edition. © 2003 by Saunders, an imprint of Elsevier, Inc. All rights reserved.
excessive growth of lanugo hair associated with internal malignancy.
Farlex Partner Medical Dictionary © Farlex 2012
hypertrichosisAn extremely rare (less 100 cases reported worldwide) excess of hair on the body, which can be generalised or localised, congenital or acquired.
• Hypertrichosis lanuginosa, possibly due to an autosomal dominant mutation on 8q;
• Generalised hypertrichosis, due to an autosomal dominant mutation on chromosome x24-q27.1;
• Terminal hypertrichosis, possibly linked to a mutation in MAP2K6 on chromosome 17;
• Circumscribed hypertrichosis;
• Localised hypertrichosis;
• Nevoid hypertrichosis.
• Hypertrichosis lanuginosa, linked to cancer, endocrinopathies and therapeutic drugs;
• Generalised hypertrichosis;
• Patterned hypertrichosis;
• Localised hypertrichosis.
Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.