E.N.T. abnormalities in arthrogryposis multiplex congenita
New Egyptian Journal of Medicine [The]. 1993; 9 (3): 943-6
em Inglês
| IMEMR
| ID: emr-30130
ABSTRACT
Arthrogryposis multiplex congenita is a congenital failure of the development of the skeletal muscles. It may be neuropathic or myopathic. Affection of the hard palate may be severe enough, especially in the myopathic type to cause otorhinolaryngology abnormalities. This may lead to disorders of speech or malfunction of the Eustachian tubes, with its sequelae, that might present to the otorhinolaryngologist and necessitate its management and follow up
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Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Músculo Esquelético
Idioma:
Inglês
Revista:
New Egypt. J. Med.
Ano de publicação:
1993
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