X-Linked Cardioskeletal Myopathy and Neutropenia
Before reading RX Patient Tools Use these quick guides before reading the article, or return to them when you need help preparing questions for a doctor....
The general Resources browser remains below. These four indexed pathways provide faster focused discovery.
Browse medical articles by letter, category, and search. Built for large health libraries.
Before reading RX Patient Tools Use these quick guides before reading the article, or return to them when you need help preparing questions for a doctor....
DefinitionX-linked Charcot–Marie–Tooth disease (often abbreviated CMTX) is a hereditary? peripheral neuropathy? that affects the insulating sheath (myelin) and the long fibers (axons) of nerves. It belongs...
DefinitionX-linked complicated corpus callosum dysgenesis is a rare genetic? condition that affects the way the corpus callosum—the wide band of nerve fibers connecting the left and...
DefinitionX-linked dominant Chondrodysplasia Punctata (CDPX1) is a rare genetic? disorder that affects bone and cartilage? development. X-Linked Dominant Chondrodysplasia Punctata (CDPX1) is a genetic condition that...
DefinitionX-linked dominant Coffin-Lowry syndrome? is a rare genetic? condition that affects how the brain, bones, and other body systems grow and work. It is present from...
DefinitionX-linked dominant congenital? hemidysplasia with ichthyosiform nevus and limb defects is usually called CHILD syndrome?. It is a very rare genetic? disease present from birth. It...
DefinitionX-Linked Dominant Disorders are a group of genetic? conditions that can affect both males and females, but they are often more severe? in males. In this...
DefinitionGlucose-6-phosphate dehydrogenase (G6PD) deficiency is a genetic? problem in red blood cells. The G6PD enzyme helps red cells make NADPH, which protects them from “oxidative” damage....
DefinitionX-linked dominant Xp11.23–p11.22 duplication syndrome? (also called Xp11.22–p11.23 duplication / microduplication syndrome) is a rare genetic? condition where a copied-extra piece (duplication) on the X-chromosome (region...
DefinitionX-Linked Endocardial Fibroelastosis (XLEF) is a rare heart condition that primarily affects infants and young children. It is important to understand the causes, symptoms, diagnosis?, and...
DefinitionThe condition recognized in the medical literature is X-linked endothelial corneal dystrophy (XECD). Despite the word “anterior” in your prompt, XECD primarily involves the posterior cornea?—especially...
DefinitionX-linked hereditary? motor and sensory neuropathy? is a long-term nerve disease that mainly damages the nerves in the legs, feet, hands, and arms. These nerves carry...