research Congenital Insensitivity to Pain with Anhidrosis and Progressing Acro-Osteolysis: A Case Report with 7-Year Follow-Up
Early intervention and protective measures are crucial for managing CIPA due to the lack of pain and standard treatment.
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research An Incompletely Penetrant Novel MAFB (p.Ser56Phe) Variant in Autosomal Dominant Multicentric Carpotarsal Osteolysis Syndrome
Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.
research Hutchinson-Gilford Progeria Syndrome: Report of 2 Cases and a Novel LMNA Mutation in China
A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.
research Risk Factors, Prevalence, and Diagnosis of Hutchinson-Gilford Syndrome with Special Reference to Case Reports
Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.
research Timed Exposure 10,600 nm CO2 Laser Drilling in Various Benign Dermal Tumors
CO₂ laser treatment is fast and effective for some benign skin tumors with minimal side effects.
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