RARE CASE REPORT - BROTHERS OF LAURENCE MOON BIEDL SYNDROME WITH GUILLAIN - BARRE SYNDROME
| Autor: | Murali Krishna Ps, Budithi Sudarsi, Nanyam Srinivasa Rao, Sapuri Sree Vani, Ravala Siddeswari |
|---|---|
| Rok vydání: | 2016 |
| Předmět: |
congenital
hereditary and neonatal diseases and abnormalities Laurence-Moon-Biedl syndrome Pediatrics medicine.medical_specialty Guillain-Barre syndrome Flaccid paralysis Polydactyly business.industry Fulminant medicine.disease nervous system diseases Retinitis pigmentosa Immunology Rare case Medicine medicine.symptom business |
| Zdroj: | Indian Journal of Case Reports. 2:4-7 |
| ISSN: | 2454-1303 2454-129X |
| DOI: | 10.32677/ijcr.2016.v02.i01.002 |
| Popis: | Laurence Moon Biedl syndrome is an autosomal recessive disorder characterized by obesity, hypogonadism, mental retardation, polydactyly, and retinitis pigmentosa. Guillain-Barre syndrome (GBS) or acute inflammatory demyelinating poly radiculo neuropathy (AIDP) is considered to be an immunological disorder with an acute and often fulminant evolution characterised by a syndrome of rapidly progressive flaccid paralysis, aflexia and albumino-cytological dissociation in the CSF. We are here with presenting case report of brothers with Laurence Moon Biedl syndrome (LBS) who presented with GBS simultaneously. |
| Databáze: | OpenAIRE |
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