by 28177pwpadmin | Nov 20, 2025 | Conditions, Neurofibromatosis Type 1, NF1, Scoliosis
Understanding NF1 and Spinal Deformity Neurofibromatosis Type 1 (NF1) is a genetic condition that affects the skin, bones, and nervous system. One of its most significant orthopedic manifestations is scoliosis; which can be dystrophic (structurally abnormal vertebrae)...
by 28177pwpadmin | Nov 13, 2025 | Conditions, Dr. Hariharan, Neurofibromatosis Type 1, NF1
Understanding NF1 and Bone Dysplasia Neurofibromatosis Type 1 doesn’t just affect nerves and skin; it also weakens the skeleton. The bones in NF1 are often fragile, with thin cortices and abnormal remodeling. These changes make fractures more likely and healing more...
by 28177pwpadmin | Nov 13, 2025 | Dr. Hariharan, Hip Dysplasia, Prader-Willi
How PWS Affects the Extremities Children with PWS often exhibit hypotonia, joint laxity, and delayed motor milestones, which can lead to orthopedic problems involving the hips, knees, and feet. Common findings include: Flat feet (pes planovalgus) from ligamentous...
by 28177pwpadmin | Nov 13, 2025 | AMC, Arthrogryposis, Dr. Hariharan, Scoliosis
Understanding Arthrogryposis and the Spine Arthrogryposis Multiplex Congenita (AMC) is a group of conditions characterized by multiple joint contractures present at birth. While the hands, feet, and limbs are often the most visibly affected, the spine is frequently...
by 28177pwpadmin | Nov 7, 2025 | Conditions, Dr. Hariharan, Prader-Willi, Scoliosis
Prader–Willi Syndrome (PWS) is a complex genetic condition caused by abnormalities in chromosome 15, leading to low muscle tone (hypotonia), growth hormone deficiency, and unique metabolic and behavioral challenges. While most discussions focus on appetite and...
