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Understanding Basaran-Yilmaz Syndrome
Basaran-Yilmaz Syndrome is a rare genetic disorder. To better understand this condition‚ let’s explore its […]
Understanding Tropical Spastic Paraparesis: Causes, Symptoms, Diagnosis, and Treatment
Article Plan⁚ Disease ─ Tropical Spastic Paraparesis Overview of Tropical Spastic Paraparesis Tropical Spastic Paraparesis […]
Understanding Cormier–Rustin–Munnich Syndrome: Symptoms, Genetic Causes, Treatment Options, Prognosis, and Research Updates
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Understanding Trochlear Dysplasia: Symptoms, Diagnosis, and Treatment
Overview of Trochlear Dysplasia Trochlear dysplasia involves a shallow, flattened trochlear groove causing patellar instability. […]
Overview of Triphalangeal Thumb Polysyndactyly Syndrome
Triphalangeal thumb-polysyndactyly syndrome (TPT-PS) is a rare congenital limb deformity with autosomal dominant inheritance. Antenatal […]
Exploring Trihydroxycholestanoylcoa Oxidase Deficiency in Peroxisomal Disorders
Introduction to Trihydroxycholestanoylcoa Oxidase Isolated Deficiency Sterol carrier protein X (SCPx) plays a crucial role […]
Understanding 2‚8 Dihydroxy-Adenine Urolithiasis: Causes, Symptoms, Diagnosis, Treatment, and Prevention
Causes of 2‚8 Dihydroxy-Adenine Urolithiasis – Genetic factors contributing to 2‚8 dihydroxy-adenine urolithiasis Some individuals […]
Understanding Ectodermal Dysplasia: Causes, Symptoms, and Treatment Options
Understanding Ectodermal Dysplasia Ectodermal Dysplasia is a genetic disorder characterized by abnormal development affecting various […]
Overview of Ectodermal Dysplasia Hypohidrotic Autosomal Dominant
Introduction to Ectodermal Dysplasia Hypohidrotic Autosomal Dominant Ectodermal Dysplasia Hypohidrotic Autosomal Dominant is a rare […]