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Considerazioni su di una famiglia con Retinosi Pigmentaria e Sindrome di Laurence-Moon-Bardet-Biedl

Published online by Cambridge University Press:  01 August 2014

L. Romei
Affiliation:
Istituto di Gcnetica Medica e Gemellologia, “G. Mendel” - Roma Clinica Oculistica dell'Università, di Roma
G. Ioli-Spada
Affiliation:
Istituto di Gcnetica Medica e Gemellologia, “G. Mendel” - Roma Clinica Oculistica dell'Università, di Roma

Summary

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A recessive pedigree of retinitis pigmentosa and Laurence-Moon-Bardet-Biedl syndrome. The retinitis affects all male children of a normal couple; the only female child shows a complete Laurence-Moon-Bardet-Biedl syndrome. The pedigree of the family shows no other case of the disease in six generations.

Zusammenfassung

ZUSAMMENFASSUNG

Stammbaum mit pigmentärer Retinose und Laurence-Moon-Bardet-Biedl Syndrome rezessiver Art. Die Retinose erscheint in allen Söhnen eines normalen Ehepares, während die einzige Tochter ein kompletes Laurence-Moon-Bardet-Biedl Syndrome entwickelt. Die genealogische Untersuchung die 6 Generationen umfasst, zeigt keine anderen Fälle dieser Krankheiten.

Sommario

SOMMARIO

Albero genealogico di retinosi pigmentaria e sindrome di Laurence-Moon-Bardet-Biedl a carattere recessivo. La retinosi compare in tutti i figli maschi di una coppia normale, mentre l'unica figlia femmina sviluppa una sindrome completa di Laurence-Moon-Bardet-Biedl. L'indagine genealogica comprendente 6 generazioni, non rivela la comparsa di altri casi della malattia.

Résumé

RÉSUMÉ

Arbre généalogique de rétinose pigmentaire et syndrome de Laurence-Moon-Bardet-Biedl du type recessif. La rétinose paraît chez tous les enfants mâles d'un couple normal tandis que la seule fille développe un syndrome complet de Laurence-Moon-Bardet-Biedl. La recherche généalogique, comprenant 6 générations, ne révèle aucun autre cas de la maladie.

Type
Research Article
Copyright
Copyright © The International Society for Twin Studies 1959

References

Bibliografia

Laurence, J.Z. and Moon, R.C.: Opht. Brit. Review 1866; 2; 3241.Google Scholar
Julia, Bell: Treas. Human Inner., 2, p. 123, Pls. 26, 1922.Google Scholar
Dax, E. C.: 1940. Quart. J. Med., 33, 263, Pl. 1.Google Scholar
Maoklin, M. T.: Can. Med. Ass., J. 1927, 17, 1191, 1336.Google Scholar
Maoklin, M. T.: J. Hered. 1936, 27, 97.CrossRefGoogle Scholar
Nettleship, E.: Opht. Review, 1907, 26, 250.Google Scholar
Scheurlen, W.: 1935 Klin. Mon. f. Augenh., 94, 761.Google Scholar
Usher, C. H.: 1935 Trans. Opht. Soc. U. K.,55, 164.Google Scholar
Von Wibaut, F.: 1931 Klin. Mon. f. Augenh., 8, 298.Google Scholar
Biedl, A.: 1922. Deut. Med. Wochens., 48, 1630.Google Scholar
François, J.: 1949. Ophthalmologica., 118, 1, 29.Google Scholar
Larmande, A. M. et Susini, R.: Bull. Soc. Opht. France, 1953. II, 81.Google Scholar
François, J. Stefens, R. et Derouck, A.: 1954. Ann. Oculist., CLXXVII, 908.Google Scholar
Dureux, J. B.: Thèse de Médecine de Nancy, 1957. I, 177.Google Scholar
Morocutti, C. e Vanni, V.: Riv. di Neurol., maggio 1959.Google Scholar
Gates, R. R.: Human Genetics. Macmillan New York, 1946.Google Scholar
Walsh, F.B.: Clinical Neuro-ophthalmology. Williams e Wilkins, Baltimore, 1957.Google Scholar