Spina Bifida: Causes, Types, Symptoms, and Treatments
Spina Bifida, often abbreviated as SB, is a congenital condition that affects the development of the spine and spinal cord….
Sickle Cell Anemia: Understanding the Disease, Its Effects, and Care Options
Sickle Cell Anemia (SCA) is a hereditary blood disorder that affects millions of people worldwide. It is characterized by abnormal…
Rett Syndrome: A Detailed Overview of Symptoms, Causes, and Care
Rett Syndrome, often abbreviated as RTT, is a rare neurodevelopmental disorder that primarily affects females. It is characterized by a…
Progeria (Hutchinson-Gilford Progeria Syndrome): Causes, Symptoms, and Care
Hutchinson-Gilford Progeria Syndrome, often abbreviated as HGPS, is an extremely rare genetic condition that causes children to age rapidly. This…
Prader-Willi Syndrome: Causes, Symptoms, and Management
Prader-Willi Syndrome, often abbreviated as PWS, is a rare genetic disorder that affects multiple systems in the body. It is…
Polycystic Kidney Disease: Causes, Symptoms, Diagnosis, and Treatment Options
Polycystic Kidney Disease, commonly abbreviated as PKD, is a genetic disorder characterized by the growth of numerous cysts in the…
Phenylketonuria (PKU): Causes, Symptoms, Diagnosis, and Management
Phenylketonuria, commonly abbreviated as PKU, is a rare genetic metabolic disorder that affects the body’s ability to break down an…
Pectus Excavatum: Understanding the Condition, Causes, Diagnosis, and Treatments
Pectus Excavatum, often abbreviated as PE, is a congenital chest wall deformity characterized by a sunken appearance of the sternum…
Osteogenesis Imperfecta: A Detailed Overview of Brittle Bone Disease
Osteogenesis Imperfecta, commonly abbreviated as OI, is a rare genetic disorder characterized by fragile bones that break easily. Often referred…
Noonan Syndrome: Causes, Symptoms, Diagnosis, and Treatment
Noonan Syndrome (NS) is a genetic disorder that affects multiple parts of the body. It is characterized by distinctive facial…