Literature DB >> 15224716

A boy with spastic paraparesis and dyspnea.

H Serap Kalkanoğlu1, Ali Dursun, Ayşegül Tokatli, Turgay Coşkun, Defne Karasimav, Haluk Topaloğlu.   

Abstract

A 4 1/2-year-old boy with signs and symptoms of spastic paraparesis and dyspnea is presented. Biotinidase deficiency was considered and was confirmed by both urine organic acid analysis and biotinidase activity measurement. The child recovered gradually on biotin therapy. Because other systemic signs and symptoms of the disease might not be present initially or might develop later, biotinidase deficiency should be considered in the differential diagnosis of a child presenting with acute or subacute spastic paraparesis.

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Year:  2004        PMID: 15224716     DOI: 10.1177/088307380401900517

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  3 in total

1.  A Treatable Cause of Myelopathy: Biotinidase Deficiency Presenting as Acute Flaccid Paralysis.

Authors:  Vykuntaraju K Gowda; Chetan Kerur; Dhananjaya K Vamyanmane; Pragalatha Kumar; Vani H Nagarajappa; Sanjay K Shivappa
Journal:  J Pediatr Genet       Date:  2020-10-08

2.  Management of anesthesia in biotinidase deficiency.

Authors:  Ugur Goktas; Muhammed Bilal Cegin; Ismail Kati; Onur Palabiyik
Journal:  J Anaesthesiol Clin Pharmacol       Date:  2014-01

3.  Severe Distal Motor Involvement in a Non-compliant Adult With Biotinidase Deficiency: The Necessity of Life-Long Biotin Therapy.

Authors:  Géraldine Van Winckel; Diana Ballhausen; Barry Wolf; Melinda Procter; Rong Mao; Patricie Burda; Davide Strambo; Thierry Kuntzer; Christel Tran
Journal:  Front Neurol       Date:  2020-10-26       Impact factor: 4.003

  3 in total

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