Biotinidase deficiency
A genetic disorder caused by mutations in the BTD gene. It is characterized by reduced or absent activity of the enzyme biotinidase which is responsible for the recycling of the vitamin biotin. Signs and symptoms appear in childhood and include seizures, hypotonia and developmental delays. If left untreated, it leads to vision and hearing loss, infections, alopecia and ataxia.
LLRM
Senior Resident
Parmarth Homeopathic Ausdhalay
M/O Incherge
Homeopathy University Jaipur
DHMS
Bangalore Medical College and Research Institute
M B B S
The Health City Hospital
Intensivist
Maharashtra University of Health Sciences Nashik
bhms
Pgimer
M.D (Pediatrics)
Medvarsity Online Limited
Family Medicine
PGIMS New OPD
Optometrists
St Jude Children's Hospital
Research Fellow
Johns Hopkins Hospital
Post doctoral fellow - Pediatric Neuroradiology
Moulana Hospital
Consultant Dermatologist & Cosmetologist
Svmc, Tirupati
Md pediatrics
Shree Krishna Hospital
Resident
Pramukhswami Medical College
MD, INTERNAL MEDICINE