Azoospermia as a new feature of Fabry disease

Author:

Papaxanthos-Roche Aline,Deminière Colette,Bauduer Frédéric,Hocké Claude,Mayer Guy,Lacombe Didier

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology,Reproductive Medicine

Reference18 articles.

1. Clinical features of and recent advances in therapy for Fabry disease;Brady;J Am Med Assoc,2000

2. Angiokeratoma corporis diffusum: Fabry’s disease;Colombi;Helv Med Acta,1967

3. α-galactosidase A deficiency: Fabry disease;Desnick,2001

4. Fabry disease, an under-recognized multisystemic disorder: expert recommendations for diagnosis, management, and enzyme replacement therapy;Desnick;Ann Intern Med,2003

5. Sequelae of storage in Fabry disease—pathology and comparison with other lysosomal storage diseases;Elleder;Acta Paediatr Suppl,2003

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