Related Experiment Video
Updated: Jan 12, 2026

07:36
Modeling Encephalopathy of Prematurity Using Prenatal Hypoxia-ischemia with Intra-amniotic Lipopolysaccharide in Rats
Published on: November 20, 2015
11.8K
Beta-ketothiolase deficiency with neurological impairment: a case report
Ibrahim Al-Sawadi1, Barah Hussain2
1Department of Physiology, İstanbul Cerrahpaşa University, İstanbul, Türkiye.
Annals of Medicine and Surgery (2012)
|November 3, 2025
Summary
Beta-ketothiolase deficiency (BKTD) is a rare metabolic disorder affecting isoleucine breakdown. Early diagnosis and management of BKTD are crucial for preventing severe complications in children.
Area of Science:
- Biochemistry
- Genetics
- Pediatrics
Background:
- Beta-ketothiolase deficiency (BKTD) is a rare inherited metabolic disorder.
- It impairs isoleucine catabolism and ketone body utilization.
- BKTD can lead to life-threatening metabolic crises if not diagnosed and managed promptly.
Related Concept Videos
Inborn Errors of Metabolism
690
Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
690
Lysosomal Hydrolases
4.4K
Lysosomes are the site for the degradation of macromolecules and biological polymers released during membrane trafficking events such as secretory, endocytic, autophagic, and phagocytic pathways. The membrane-enclosed area of the lysosome, called the lumen, contains hydrolytic enzymes active in an acidic environment. These acid hydrolases are functional at a pH between 4.5 and 5 and are involved in cellular processes such as cell signaling, energy metabolism, restoration of the plasma membrane,...
4.4K
Protein Import into the Peroxisomes
5.2K
Cells contain membrane-bound organelles called peroxisomes that oxidize organic molecules by transferring hydrogen atoms to oxygen, producing hydrogen peroxide. Peroxisomes enzymatically convert the released hydrogen peroxide into water and oxygen.
Peroxisomal Protein Import:
Peroxisomes lack the genetic machinery required to code for their own proteins. Hence, most peroxisomal membrane, lumenal and transmembrane proteins are synthesized in the cytoplasm or ER and transported to the peroxisome...
Peroxisomal Protein Import:
Peroxisomes lack the genetic machinery required to code for their own proteins. Hence, most peroxisomal membrane, lumenal and transmembrane proteins are synthesized in the cytoplasm or ER and transported to the peroxisome...
5.2K
Pedigree Analysis
88.7K
Overview
88.7K
ATP Synthase: Structure
15.1K
ATP synthase or ATPase is among the most conserved proteins found in bacteria, mammals, and plants. This enzyme can catalyze a forward reaction in response to the electrochemical gradient, producing ATP from ADP and inorganic phosphate. ATP synthase can also work in a reverse direction by hydrolyzing ATP and generating an electrochemical gradient. Different forms of ATP synthases have evolved special features to meet the specific demands of the cell. Based on their specific feature, ATP...
15.1K

