MSUD
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MSUD — • maple syrup urine disease … Dictionary of medical acronyms & abbreviations
MSUD — biomed. abbr. Maple Syrup Urine Disease … United dictionary of abbreviations and acronyms
Maple syrup urine disease (MSUD) — Hereditary disease due to deficiency of an enzyme involved in amino acid metabolism, characterized by urine that smells like maple syrup … Medical dictionary
Maple syrup urine disease — Classification and external resources Isoleucine (pictured above), leucine, and valine are the branched chain amino acids that build up in MSUD. ICD … Wikipedia
metabolic disease — ▪ pathology Introduction any of the diseases or disorders that disrupt normal metabolism, the process of converting food to energy on a cellular (cell) level. Thousands of enzymes participating in numerous interdependent metabolic pathways… … Universalium
Dentate nucleus — This article is about the dentate nucleus. For other dentate, see Dentate. Brain: Dentate nucleus Sagittal section through right cerebellar hemisphere. The right olive has also been cut sagitally. (Dentate nucleus labeled at top.) Latin nucleus… … Wikipedia
BCKDHB — Branched chain keto acid dehydrogenase E1, beta polypeptide (maple syrup urine disease), also known as BCKDHB, is a human gene.cite web | title = Entrez Gene: BCKDHB branched chain keto acid dehydrogenase E1, beta polypeptide (maple syrup urine… … Wikipedia
Maladie du sirop d'érable — Référence MIM 248600 Transmission Récessive Chromosome 19q13.1 q13.2 6p22 p21 1p31 7q31 q32 Gène BCKDHA BCKDHB DBT GCSL … Wikipédia en Français
Dihidrolipoil deshidrogenasa — Saltar a navegación, búsqueda Estructura 3D de tres unidades de dihidrolipoildeshidrogenasa. PDB 1ZMC … Wikipedia Español
Newborn screening — See also: Apgar score Newborn screening Intervention MeSH D015997 Newborn screening is the process by which infants are screened shortly after birth for a list of disorders that are treatable, but di … Wikipedia
