Endocrine abnormalities in two siblings with Rothmund Thomson Syndrome
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Heighten Science Publications Corporation
Link
https://www.endometaboljournal.com/articles/acem-aid1010.pdf
Reference10 articles.
1. 1. Kitao S, Shimamoto A, Goto M, Miller RW, Smithson WA, Lindor NM, et al. Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome. Nat Genet. 1999; 22: 82-84. Ref.: https://goo.gl/AdkJ5R
2. 2. Bloch B, Stauffer H. Poikiloderma-like changes in connection with underdevelopment of the sexual glands and dystrophia adiposogenitalis. Archives of Dermatology and Syphilology. 1929; 19: 22-34. Ref.: https://goo.gl/swFK9A
3. 3. Vennos EM, Collins M, James WD. Rothmund-Thomson syndrome: review of the world literature. J Am Acad Dermatol. 1992; 27: 750-759. Ref.: https://goo.gl/oq8ij4
4. 4. Werder EA, Mürset G, Illig R, Prader A. Hypogonadism and parathyroid adenoma in congenital poikiloderma (Rothmund-Thomson syndrome). Clin Endocrinol. 1975; 4: 75-82. Ref.: https://goo.gl/hnWH3Y
5. 5. Guyda H, MacLeod P, Colle E. Endocrine Aspects of the Rothmund-Thomson syndrome. Pediatric Research. 1975; 9: 689. Ref.: https://goo.gl/WZYpX3
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