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Rothmund-Thomson Syndrome
(Poikiloderma Congenitale)
An autosomal recessive syndrome occurring principally in females, characterized by the presence of reticulated, atrophic, hyperpigmented, telangiectatic cutaneous plaques, often accompanied by juvenile cataracts, saddle nose, congenital bone defects, disturbances in the growth of hair; nails; and TEETH; and hypogonadism.
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 Rothmund-Thomson syndrome atlasgeneticsoncology.org |  Rothmund-Thomson Syndrome www.dermis.net |  Rothmund-Thomson syndrome dermnetnz.org |  Rothmund-Thomson syndrome is a www.i-am-pregnant.com |
 Rothmund-Thomson Syndrome www.dermis.net |  Picture of Rothmund-Thomson www.medicinenet.com |  Rothmund-Thomson. Syndrome www.dermaamin.com |  Rothmund–Thomson syndrome en.wikipedia.org |
Diagnosis and therapies
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Wikipedia
Poikiloderma, Rapadilino syndrome, Kindler syndrome, Hans Kindler, Robert A. Kindler, Beard v. Kindler, Jeff Kindler, Damian Kindler, Kindler, Kindler v. Canada (Minister of Justice)
More information
- Reported cases - Summary of cases reported on this disease.
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- WHO - World Health Organization.
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- MeSH - Medical Subject Headings.
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