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Osservazioni su una coppia di fratelli mononati, affetti da epidermolisi bollosa semplice e da poliomielite anteriore acuta

Published online by Cambridge University Press:  01 August 2014

D. Gionta
Affiliation:
Clinica delle Malattie infettive dell'Università di Roma
R. Marioni
Affiliation:
Clinica delle Malattie infettive dell'Università di Roma

Summary

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The authors have described two brothers, both affected by epidermolysis bullosa, struck at the same time by poliomyelitis anterior acuta having identical paralytic manifestations concerning the lower limbs and an almost reversed asymmetrical affection concerning the muscular groups of the upper limbs. Owing to the presence of a congenital desease, the Authors have considered the existence in the above mentioned brothers of a particular predisposition also for poliomyelitic infection.

Riassunto

Riassunto

Gli AA. hanno descritto una coppia di fratelli mononati, ambedue affetti da epidermolisi bollosa semplice, colpiti contemporaneamente da poliomielite anteriore acuta, con identiche manifestazioni paralitiche a carico degli arti inferiori e interessamento quasi speculare dei gruppi muscolari degli arti superiori. Data la presenza di una malattia congenita, hanno pensato che potesse esistere nella coppia descritta un particolare terreno predisponente anche per l'infezione poliomielitica.

Résumé

RÉSUMÉ

Les auteurs ont décrit deux frères, tous les deux affectés d'épidermolyse huileuse simple, atteints en même temps de poliomyélite antérieure aiguë, ayant exactement les mêmes manifestations paralitiques aux extrémités inférieures et une affection presque spéculaire des groupes musculaires des extrémités supérieures. Étant donné la présence d'une maladie congénitale, les auteurs ont aussi pensé à l'existence d'une particulière prédisposition à l'infection poliomyélitique dans le couple en question.

Zusammenfassung

ZUSAMMENFASSUNG

Die Verfasser beschreiben zwei Brüder, beide mit einfacher Epidermolisis bullosa behaftet und gleichzeitig mit Poliomyelitis anterior acuta befallen mit identischen paralystischen Erscheinungen der unteren Gliedmassen und fast spiegelartiger Affektion der muskulären Gruppen der oberen Gliedmassen. Wegen Anwesenheit einer kongenitalen Kränkelt, haben die Verfasser die Möglichkeit einer besonderen Empfänglichkeit des obenerwähntes Paar für poliomyelitische Infektion berücksichtigt.

Type
Research Article
Copyright
Copyright © The International Society for Twin Studies 1960

References

Bibliografia

Addair, J., Snyder, L. H.: J. Hered., 33, 307, 1942.Google Scholar
Angela, G. C., Polistina, G.: G. Mal. Inf. Parass., 6, 3, 1954.Google Scholar
Aycock, W. L.: Am. J. Med. Sc., 203, 452, 1943.Google Scholar
Aycock, W. L.: Am. J. Med., Sc. 202, 456, 1942.Google Scholar
Borgstrom, C. A.: Finska läk – sallsk. handl., 81, 33, 1938.Google Scholar
Caronia, G.: Le più comuni malattie infettive acute, ed. Vallardi-Milano, 540, 1946.Google Scholar
Gerutti, : Giorn. It. di Dermat. e Sifil., 2, 335, 1933.Google Scholar
Cockayne, E. A.: Oxford University Press, 118, 1933.Google Scholar
Czickeli, H.: Schweiz. med. Woch., 44, 1092, 1948.Google Scholar
Dadone, G.: Mal. Inf. Parass., 6, 331, 1954.Google Scholar
De Toni, G.: Forze Sanitarie, 17, 1187, 1939.Google Scholar
De Toni, G.: Il Lattante, 1, 319, 1939.Google Scholar
Draper, : Am. Journ. Of Med. Scien., 1932.Google Scholar
Farmer, A. D.: M. J. Australia, 1, 141, 1955.Google Scholar
Gautier, P.: Praxis, 31, 29, 1942.Google Scholar
Herndorn, C., Jennings, R.: Am. J. human Genet., 3, 17, 1951.Google Scholar
Hnevkovsky, R.: Casop. Lek. Cesk. 88, 1328, 1949.Google Scholar
Hofmeier, K.: Erbartz. 1, 11, 1938.Google Scholar
Hofmeier, K.: Kinderärztlieck. Prax. 9, 20, 1938.Google Scholar
Imperato, C.: La Pediatria, 5-6, 389, 1953.Google Scholar
Imperato, C.: Relazione al XXIII Congr. Ital. di Pediatria, Bologna, Sett. 1954.Google Scholar
Marcozzi, : Arch. It. Derm. Sif. e Ven., 6, 555, 1929.Google Scholar
Masini, T.: Folia Hered. Path., 2, 115, 1953.Google Scholar
Mengoli, : Riv. Clin. Med., 1940.Google Scholar
Messeri, E.: Riv. Clin. Ped., 44, 100, 1946.Google Scholar
Morley, : Brit. Journ. of Derm., 35, 1914.Google Scholar
Pasini, A.: Giorn. It. Derm, e Sif., 9, 558, 1928.Google Scholar
Pasini, A.: Giorn. It. Derm, e Sif., 73, 125, 1932.Google Scholar
Pasini, A.: Boll. Reg. Soc. It. Derm, e Sif, 1, 401, 1932.Google Scholar
Ritossa, P.: Agg. Ped., 4, 193, 1953.Google Scholar
Roach, R. D.: Canad. M. A. J., 55, 122, 1946.Google Scholar
Scarpa, A.: Giorn. It. di Derm, e Sif., 74, 67, 1933.Google Scholar
Stephens, H. D.: Int. Med. Journ. Austr., 13, 57, 1908.Google Scholar
Stokes, J. Jr.: Text. book, of Pediatrics Philadelphia and London, 1950.Google Scholar
Taylor, J. M.: Phil. Med. Journ., 1, 208, 1898.Google Scholar
Teodori, U., Borghi, A., Neri Serneri, G.: Eredità e localizzazioni morbose. Ed. Omnia Medica. Pisa. 1955.Google Scholar
Tolentino, P.: La Pediatria, 48, 657, 1940.Google Scholar
Wickman, I.: Nerv. Ment. Dis. suppl., 16, 1913.Google Scholar
Wise, : New York Derm. Soc., 24 oct. 1922.Google Scholar
Yoshida, Y. J.: Exp. Med., 53, 2, 1950.Google Scholar