Triple X Syndrome: Causes, Diagnosis and Treatment Triple X syndrome, also known as trisomy X or 47, XXX, is a rare genetic condition that affects females. This chromosomal disorder is characterized by an extra X chromosome, resulting in three X chromosomes instead of the typical two. First identified in the 1950’s, Triple X syndrome … Read more
Exploring the Wonders of Savant Syndrome Savant syndrome, an extraordinary and rare cognitive phenomenon, is a condition where individuals exhibit remarkable abilities in specific domains, juxtaposed against cognitive or developmental deficits in other areas. Discovered in the late 19th century, this enigmatic condition has captivated the scientific community with its profound implications for understanding the … Read more
What Is Schilder’s Disease? Schilder’s Disease, also known as diffuse myelinoclastic sclerosis, is a rare demyelinating disorder primarily affecting the central nervous system. This enigmatic condition was first identified by Paul Ferdinand Schilder, a Dutch neurologist, in the early 20th century. The discovery of Schilder’s Disease marked a significant advancement in neurology, shedding light … Read more
Prosopagnosia: Symptoms, Causes and Treatment Prosopagnosia is a rare neurological condition that affects an individual’s capability to recognize familiar faces, including those of their close friends and family members. This perplexing disorder falls under visual agnosias, where specific visual information processing is impaired despite intact basic visual perception. Prosopagnosia is a peculiar condition … Read more
Ellis-van Creveld Syndrome Ellis-van Creveld Syndrome (EvC) is a rare mental disorder. It is also enigmatic genetic disorder which reveals a captivating interplay of anomalies that set it apart in the medical landscape. Characterized by the elusive fusion of chondrodysplasia and ectodermal dysplasia, this condition manifests with a distinct cluster of skeletal and dental abnormalities, … Read more
