"Rothmund-Thomson Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
- Rothmund-Thomson Syndrome
- Rothmund Thomson Syndrome
- Syndrome, Rothmund-Thomson
- Poikiloderma Congenitale of Rothmund-Thomson
- Poikiloderma Atrophicans and Cataract
- Congenital Poikiloderma
- Poikiloderma Congenitale
- Congenitale, Poikiloderma
- Congenitales, Poikiloderma
- Poikiloderma Congenitales
- Poikiloderma of Rothmund-Thomson
- Poikiloderma of Rothmund Thomson
- Rothmund-Thomson Poikiloderma
- Rothmund-Thomson Poikilodermas
Below are MeSH descriptors whose meaning is more general than "Rothmund-Thomson Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Rothmund-Thomson Syndrome".
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