Overview of Scleromyxedema Papular mucinosis, also known as scleromyxedema, is a rare skin disorder characterized […]
Understanding Microcephaly with Normal Intelligence and Immunodeficiency: A Genetic Disorder Overview
Introduction Nine patients with a new genetic disorder⁚ microcephaly with normal intelligence‚ bird-like facial appearance‚ […]
Understanding Microcephaly-Microcornea Syndrome, Seemanova Type
Introduction Microcephaly-microcornea syndrome, Seemanova type is a rare condition characterized by specific physical features and […]
Understanding the Complexities of Microcephaly, Mental Retardation, Spasticity, and Epilepsy
Introduction Information on the topic ″Disease⁚ Microcephaly mental retardation spasticity epilepsy″ discusses various genetic and […]
Understanding Cantu-Sanchez-Corona-Garcia Syndrome: Causes, Symptoms, Diagnosis, and Treatment
Causes of Cantu-Sanchez-Corona-Garcia Syndrome The primary cause of Cantu-Sanchez-Corona-Garcia Syndrome is attributed to genetic mutations. […]
Understanding Atopic Dermatitis
Understanding Atopic Dermatitis Causes of Atopic Dermatitis Atopic dermatitis, also known as eczema, can be […]
Understanding Congenital Heart Block: Causes, Symptoms, and Management
Understanding Congenital Heart Block Introduction Congenital Heart Block is a serious cardiac condition that affects […]
Understanding Adrenoleukodystrophy: Symptoms, Treatment Options, and Genetic Counseling
Understanding Adrenoleukodystrophy involves recognizing its symptoms‚ exploring treatment options‚ and genetic counseling. Symptoms of Adrenoleukodystrophy […]
Overview of Primary Hyperoxaluria
The accumulation of oxalate in the kidneys and other organs characterizes primary hyperoxaluria, a rare […]
Management of Primary Hyperparathyroidism
Introduction to Primary Hyperparathyroidism Primary hyperparathyroidism is a relatively common endocrine disorder characterized by hypercalcemia […]