→ Chondrodysplasia Punctata 1 (X-Linked)

→ Chondrodysplasia Punctata 1 (X-Linked)

Back to Previous Chondrodysplasia Punctata 1 (X-Linked) X-linked chondrodysplasia punctata 1 is a disorder of cartilage and bone development that occurs almost exclusively in males. Chondrodysplasia punctata is an abnormality that appears on x-rays as spots...
→ Chondrodysplasia Punctata 1 (X-Linked)

→ Chondrodysplasia Punctata 2 (X-Linked)

Back to Previous Chondrodysplasia Punctata 2 (X-Linked) X-linked chondrodysplasia punctata 2 is a disorder characterized by bone, skin, and eye abnormalities. It occurs almost exclusively in females. Although the signs and symptoms of this condition vary widely,...
→ Chondrodysplasia Punctata 1 (X-Linked)

→ Choroideremia

Back to Previous Choroideremia Choroideremia is a genetic disorder of sight that usually affects males. Female carriers may have mild symptoms without loss of vision. Major symptoms are difficulty seeing in the dark leading to progressive loss of peripheral vision,...
→ Chondrodysplasia Punctata 1 (X-Linked)

→ Christianson Syndrome

Back to Previous Christianson syndrome Christianson syndrome is an X-linked syndrome associated with intellectual disability, microcephaly, seizures, ataxia, and absent speech. Many individuals with this condition have a happy demeanor with frequent smiling and...
→ Chondrodysplasia Punctata 1 (X-Linked)

→ Chronic Granulomatous Disease

Back to Previous Chronic Granulomatous Disease Chronic granulomatous disease (CGD) is a rare inherited primary immune deficiency disorder that affects certain white blood cells (neutrophils, monocytes, macrophages, eosinophils). The disorder is characterized by an...