Comunicación Nº: 057 | English version |
Lucía Hernández, Santiago Madero, Ángel Castaño, Elvira Martínez, Miguel Gallego
[Título] [Introducción] [Material y Métodos] [Resultados] [Iconografía] [Discusión] [Comentarios]
1.- Schuster V., Eschenhagen T., Kruse K., Gierschik P., Kreth H.W. Endocrine and molecular biological studies in a German family with Albrigth hereditary osteodystrophy. Eur J Pediatr 1993; 152:185-189.
2.- Patten J.L, Jhons D.R., Valle D. et al. Mutation in the gene encoding the stimulatory G pprotein of adenylate cyclase in Albrights hereditary osteodystrophy. N Engl J Med 1990; 322:1412-1419.
3.- Phelan MC, Rogers RC, Clarkson KB,et al. Albright hereditary osteodystrophy and del (2) (q37.3) in four unrelated individuals. Am J Med Genet 199531, 58:1-7.
4.- Koo BB., Schwindinger WF., Levine MA. Characterization of Albright hereditary osteodystrophy and related desorders.Acta Paediatr Sin 1995;36:3-13.
5.- Levine MA., Downs RW .,Moses AM. , et al. Resistence to multiple hormones in patients with pseudohypoparathyroidism and deficient guanine nucleotide regulatory protein. Am J Med 74: 545-556.
6.- Levine MA., Jap TS., Hung W. Infantile hypothyroidism in two sibs: an unusual presentation of pseudohypoparathyroidism type Ia. J Pediatr1983;107 :919-922.
7.- Miller ES; Esterly NB., Fairley J.A. Progressive osseous heteroplasia. Arch Dermatol 1996;132:787-791.
8.- Goodman R.M., Gorlin R:J:. Malformaciones en el lactante y en el niño. Barcelona, 1986. Salvat.
9.- Izraeli S, Metzker A, Horev G, Karmi D, Merlob P, Farfel Z. Albright hereditary osteodystrophy with hypothyroidism, normocalcemia and normal Gs protein activity: a family presenting with congenital osteoma cutis. Am J Med Genet 1992;43:764-7.
10.- Lever WF, Schaumburg-Lever G. Histopathology of the skin, 7ª edición. Philadelphia, 1990, J.B. Lippincott Co.
11.- Prendiville JS., Lucky AW., Mallory SB., Mughal Z ., Miouni F., Langman CB. Osteoma cutis as presenting sign of pseudohypoparathyroidism. Pediatr Dermatol 1992;9:11-18.