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Cerebrotendinous xanthomatosis
Cerebrotendinous xanthomatosis is a rare autosomal recessive lipid storage disorder affecting the biosynthetic pathway of bile acids, leading to increased cholestanol formation and its accumulation in various tissues. Patients can present with tendon xanthomas, gait abnormalities, osteoporosis with...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654472/ https://www.ncbi.nlm.nih.gov/pubmed/23682184 http://dx.doi.org/10.4103/0019-5413.108918 |
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author | Vadapalli, Satyadev |
author_facet | Vadapalli, Satyadev |
author_sort | Vadapalli, Satyadev |
collection | PubMed |
description | Cerebrotendinous xanthomatosis is a rare autosomal recessive lipid storage disorder affecting the biosynthetic pathway of bile acids, leading to increased cholestanol formation and its accumulation in various tissues. Patients can present with tendon xanthomas, gait abnormalities, osteoporosis with or without a pathological fracture, diminished vision, intractable diarrhoea, seizures, ataxia, psychosis, and mental retardation. We report a 20-year-old man who presented with multiple recurrent tendon swellings and seizures. The earlier diagnosis and treatment helps in preventing the devastating neurological sequalae of this sinister condition. Treatment with chenodeoxycholic acid is crucial in preventing the progression of this rare disorder. |
format | Online Article Text |
id | pubmed-3654472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-36544722013-05-16 Cerebrotendinous xanthomatosis Vadapalli, Satyadev Indian J Orthop Case Report Cerebrotendinous xanthomatosis is a rare autosomal recessive lipid storage disorder affecting the biosynthetic pathway of bile acids, leading to increased cholestanol formation and its accumulation in various tissues. Patients can present with tendon xanthomas, gait abnormalities, osteoporosis with or without a pathological fracture, diminished vision, intractable diarrhoea, seizures, ataxia, psychosis, and mental retardation. We report a 20-year-old man who presented with multiple recurrent tendon swellings and seizures. The earlier diagnosis and treatment helps in preventing the devastating neurological sequalae of this sinister condition. Treatment with chenodeoxycholic acid is crucial in preventing the progression of this rare disorder. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3654472/ /pubmed/23682184 http://dx.doi.org/10.4103/0019-5413.108918 Text en Copyright: © Indian Journal of Orthopaedics http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Vadapalli, Satyadev Cerebrotendinous xanthomatosis |
title | Cerebrotendinous xanthomatosis |
title_full | Cerebrotendinous xanthomatosis |
title_fullStr | Cerebrotendinous xanthomatosis |
title_full_unstemmed | Cerebrotendinous xanthomatosis |
title_short | Cerebrotendinous xanthomatosis |
title_sort | cerebrotendinous xanthomatosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654472/ https://www.ncbi.nlm.nih.gov/pubmed/23682184 http://dx.doi.org/10.4103/0019-5413.108918 |
work_keys_str_mv | AT vadapallisatyadev cerebrotendinousxanthomatosis |