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2004, Number 4

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Gac Med Mex 2004; 140 (4)

A 32-Year-Old Woman with Cephalea, Galactorrhea, Prognatism, and Acral Growth.

Cheng-Oviedo S, Espinosa DAL, Mercado M, Sandoval C

Language: Spanish
References: 10
Page: 449-454
PDF size: 70.84 Kb.


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REFERENCES

  1. Melmed S. Acromegaly. In: Melmed S, editor. The Pituitary. Blackwell Science;1995. pp. 413-442.

  2. Gadelha M, Prezant T, Une K, Glick R, Moskal II S, Vaisman M, Melmed S. Loss of heterozygocity on chromosome 11q13 in two families with acromegaly/gigantism is independent of mutations of the MEN-1 gene. J Clin Endocrinol Metab 1999;84:249-256.

  3. Teh BT, Kytola S, Farnebo F, Bergman L, Wong FK, Weber G, et al. Mutation analysis of the MEN-1 gene in multiple endocrine neoplasia type1, familial acromegaly and familial isolated hyperpathyroidism. Clinical Diagnosis Group: Mutation Analysis Group. J Clin Endocrinol Metab 1998;83:2621-2626.

  4. Brandi M, Gagel R, Angeli A, Bilezikian J, Beck-Peccoz P, Bordi C, et al. Guidelines for diagnosis and therapy of MEN type 1 and type 2. J Clin Endocrinol Metab 2001;86(12):5658-5671.

  5. Guo S, Sawicki M. Molecular and genetic mechanisms of tumorigenesis in multiple endocrine neoplasia type-1. Mole Endocrinol 2001;15(10):1653-1664. 6. Stratakis C, Kirschner L, Carney A. Clinical and molecular features of the Carney complex: diagnostic criteria and recommendations for patient evaluation. J Clin Endocrinol Metab. 2001;86(9):4041-4046.

  6. Gadelha M, Une K, Rohde K, Vaisman M, Kineman R, Forman L. Isolated familial somatotropinomas: establishment of linkage to chromosome 11q13.1-11q13.3 and evidence for a potential second locus at chromosome 2p16-12. J Clin Endocrinol Metab 2000;85(2):707-714.

  7. Matyakhina L, Pack S, Kirschner L, Pak E, Mannan P, Jaikumar J, Taymans S, Sandrini F, Carney J, Stratakis C. Chromosome 2 (2p16) abnormalities in Carney complex tumours. J Med Genet 2003;40:268-277

  8. De Menis E, Prezant T. Isolated familial somatotropinomas: clinical features and analysis of the MEN-1 gene. Pituitary 2002;5:11-15.

  9. Yamada S, Yoshimoto S. Inactivation of tumor supressor gene on 11q13 in two brothers with familial acrogigantism without MEN-1. J Clin Endocrinol Metab 1997;82:239.

  10. Jorge B, Agarwal S, Lando V, Salvatori R, Barbero R, Abelin N, et al. Study of the multiple endocrine neoplasia type 1 growth hormone-releasing hormone receptor, Gsá, and Gi2á genes in isolated familial acromegaly. J Clin Endocrinol Metab. 2001;86:542-544.




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