{"id":164621,"date":"2022-06-12T07:51:46","date_gmt":"2022-06-12T07:51:46","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=164621"},"modified":"2022-06-12T08:01:38","modified_gmt":"2022-06-12T08:01:38","slug":"biotinidase-deficiency","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/biotinidase-deficiency\/","title":{"rendered":"Biotinidase deficiency"},"content":{"rendered":"

An autosomal recessive disease in which affected children fail to metabolize biotin effectively. Seizures, encephalopathy, neurodevelopmental delay, spasticity or diminished muscle tone, paresis, visual disturbances, deafness, skin rash, and hair loss commonly occur. Immediate ongoing treatment with supplemental biotin can effectively suppress the symptoms of this disease.<\/p>\n

\n

 <\/p>\n","protected":false},"excerpt":{"rendered":"

An autosomal recessive disease in which affected children fail to metabolize biotin effectively. Seizures, encephalopathy, neurodevelopmental delay, spasticity or diminished muscle tone, paresis, visual disturbances, deafness, skin rash, and hair loss commonly occur. Immediate ongoing treatment with supplemental biotin can effectively suppress the symptoms of this disease.  <\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[2],"tags":[],"class_list":["post-164621","post","type-post","status-publish","format-standard","hentry","category-b"],"yoast_head":"\nBiotinidase deficiency - Definition of Biotinidase deficiency<\/title>\n<meta name=\"description\" content=\"An autosomal recessive disease in which affected children fail to metabolize biotin effectively. 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