Case Study of Bardet-Biedl Syndrome with Fetal Lobulation and Focal Segmental Glomerulosclerosis
Bardet-Biedl syndrome is a genetic autosomal recessive disease characterized by abdominal obesity, mental retardation, dysmorphic extremities, retinal dystrophy or pigmentary retinopathy, hypogonadism or hypogenitalism, and kidney involvement. Patients with renal involvement may present with both st...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Turkiye Klinikleri
2008-05-01
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| Series: | Turkish Journal of Endocrinology and Metabolism |
| Subjects: | |
| Online Access: | http://www.turkjem.org/eng/yazilar.asp?yaziid=554&sayiid= |