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An Med Interna ; 19(9): 460-2, 2002 Sep.
Article in Spanish | MEDLINE | ID: mdl-12420631

ABSTRACT

Primay ciliary dyskinesia is a rare autosomal recessive disorder, characterized by abnormal ciliary structure and function and chronic lung, sinus and middle ear disease. A 45-year-old man with a history of recurrent respiratory infections, which was developped in the adult age, and was presented with moderate clinical involvement, and spermatic hypomotility in seminogram. Diagnosis and differential diagnosis was based on the typical clinical picture and the electron microscopical demonstration of ultrastructural abnormalities. We found abnormal number of cilia on the bronchial mucosa cells and the ciliary structure was abnormal too. We observed abnormally short dynein arms and defective radial spokes.


Subject(s)
Ciliary Motility Disorders/diagnosis , Ciliary Motility Disorders/pathology , Diagnosis, Differential , Humans , Male , Middle Aged
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