Penetrating trauma is an injury that occurs when an object pierces the skin and enters a tissue of the body creating an open wound. In blunt or non-penetrating trauma there […]
List of articles in "Disease" category - Page 232
Little League elbow
Little League elbow is a condition that is caused by repetitive throwing motions especially in children who play sports that involve an overhand throw.The name of the condition is derived […]
Galactose epimerase deficiency
Galactose epimerase deficiency also known as GALE deficiency Galactosemia III and UDP-galactose-4-epimerase deficiency is a rare autosomal recessive form of galactosemia associated with a deficiency of the enzyme galactose epimerase.
Dubowitz syndrome
Dubowitz syndrome is a rare genetic disorder characterized by microcephaly growth retardation and a characteristic facial appearance (small round triangular shaped with a pointed receding chin a broad wide-tipped nose […]
D-bifunctional protein deficiency
D-Bifunctional protein deficiency (officially called 17-β-hydroxysteroid dehydrogenase IV deficiency) is an autosomal recessive peroxisomal fatty acid oxidation disorder. Peroxisomal disorders are usually caused by a combination of peroxisomal assembly defects […]
Learning disability
Learning disability is a classification including several areas of functioning in which a person has difficulty learning in a typical manner usually caused by an unknown factor or factors.While learning […]
DeSanctis–Cacchione syndrome
DeSanctis–Cacchione syndrome is an extremely rare disorder characterized by the skin and eye symptoms of xeroderma pigmentosum (XP) occurring in association with microcephaly progressive mental retardation retarded growth and sexual […]
Pneumaturia
Pneumaturia is the passage of gas or air in urine. This may be seen or described as bubbles in the urine.
Cholinergic urticaria
Cholinergic urticaria (CU) is one of the physical urticaria (commonly referred to as hives) which is provoked during sweating events.
3C syndrome
3C syndrome also known as CCC dysplasia Craniocerebellocardiac dysplasia or Ritscher–Schinzel syndrome is a rare condition whose symptoms include heart defects cerebellar hypoplasia and cranial dysmorphism. It was first described […]