Rett syndrome is a rare genetic disorder marked by abnormal development of the brain. Females are predominantly affected by the condition than males. In the initial phases of growth post birth, Rhett syndrome babies tend to elicit normal development. The adverse symptoms of the condition are typically observed six months after delivery. As the affected… Continue reading Rett Syndrome
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Myelodysplastic Syndrome
Formerly called pre-leukemia, myelodysplastic syndrome or MDS refers to a group of hematological ailments that occur due to abnormal production or functioning of the myeloid blood cells, i.e., malformed or malfunctioning blood cells. Myelodysplastic syndrome primarily manifests as anemia because of reduced RBC production. Blood cells are made in the bone marrow. Any kind of… Continue reading Myelodysplastic Syndrome
Duchenne Muscular Dystrophy
Named after Dr. Duchenne de Boulogne, Duchenne muscular dystrophy is a genetic condition marked by degeneration of the muscles. It is a part of a group of 20 hereditary conditions known as muscular dystrophy and Duchenne muscular dystrophy is the most common. It is more prevalent in males than females. Duchenne muscular dystrophy is caused… Continue reading Duchenne Muscular Dystrophy
Down Syndrome
Also called Trisomy 21, Down syndrome is a congenital genetic disorder marked by developmental delays, mental retardation, and other abnormalities. The severity of the condition varies from one patient to another; hence the associated disabilities also tend to vary between patients, from moderate to extreme. Risk Factors Down syndrome is caused due to presence of… Continue reading Down Syndrome