𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Encephalopathy, hearing loss and retinal occlusions (Susac’s syndrome): a new case

✍ Scribed by M. Maddestra; S. Sabatini; A. Paci

Publisher
Springer Milan
Year
1998
Tongue
English
Weight
520 KB
Volume
19
Category
Article
ISSN
1590-1874

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Susac's syndrome: Intratympanic therapy
Susac's syndrome: Intratympanic therapy for hearing loss and a review of the literature
✍ Brianna K. Crawley; Abby Close; Cecilia Canto; Jeffrey P. Harris 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 65 KB

## Abstract Two cases of Susac's Syndrome are presented with a discussion of treatment modalities for the associated severe sensorineural deafness. Patients were managed with high dose oral steroids, anticoagulants and immunosuppressive drugs. The addition of intratympanic methylprednisolone inject

Apparently new syndrome of sensorineural
Apparently new syndrome of sensorineural hearing loss, retinal pigment epithelium lesions, and discolored teeth
✍ Innis, Jeffrey W.; Sieving, Paul A.; McMillan, Pamella; Weatherly, Robert A. 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 58 KB 👁 2 views

We report on a family with early-onset sensorineural hearing loss, abnormal retinal pigment epithelium granularity, accumulation of creamy-white lesions at the level of the retinal pigment epithelium particularly superior to the arcade, and selective discoloration (brown) of molars or canine deciduo

New autosomal recessive syndrome of prog
New autosomal recessive syndrome of progressive sensorineural hearing loss and cataracts: Report on two Brazilian patients
✍ De Vitto, L. P. M.; Costa, O. A.; Bevilaqua, M. C.; Passerotti, S.; Richieri-Cos 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 718 KB

We report on two sisters with cataracts and progressive sensorineural hearing loss, starting in infancy. They were born to consanguineous parents, and there were no similar cases in the family. To our knowledge this is the first report on this autosomal recessive condition. Clinical and genetic aspe