Introduction Congenital scoliosis with unilateral unsegmented bar remains a surgical challenge‚ requiring careful consideration of […]
Understanding Albright’s Hereditary Osteodystrophy: Symptoms, Causes, Diagnosis, and Treatment
Symptoms of Albright’s Hereditary Osteodystrophy Albright’s Hereditary Osteodystrophy symptoms include short stature‚ obesity‚ rounded face‚ […]
Understanding Sclerosteosis: Genetic Basis, Clinical Features, and Radiological Manifestations
Overview of Sclerosteosis Sclerosteosis is a rare, severe sclerosing bone dysplasia characterized by progressive skeletal […]
Understanding Microcephaly, Mental Retardation, and Retinopathy: Syndromes, Diagnosis, and Management
Article Plan⁚ Disease — Microcephaly Mental Retardation Retinopathy Introduction to Microcephaly, Mental Retardation, and Retinopathy […]
Understanding Galloway-Mowat Syndrome: Characteristics, Diagnosis, and Management
Introduction The Galloway-Mowat syndrome is a rare inherited disorder characterized by microcephaly, hiatus hernia, and […]
Overview of Scott Syndrome
Scott syndrome is an extremely rare inherited hemorrhagic disorder linked to the lack of exposure […]
Understanding Microcephaly Cleft Palate Autosomal Dominant Disorder
Overview of Microcephaly Cleft Palate Autosomal Dominant Disorder Say et al․ (1975) described a new, […]
Understanding Atopic Conjunctivitis: Causes, Symptoms, Treatment, and Prevention
Causes of Atopic Conjunctivitis Atopic conjunctivitis can be triggered by environmental factors or genetic predisposition. […]
Understanding Microcephaly-Cardiac Defect-Lung Malsegmentation Syndrome
Introduction Microcephaly-cardiac defect-lung malsegmentation syndrome is a very rare condition characterized by distinct features affecting […]
Understanding SCOT Deficiency: Causes, Symptoms, and Management
Introduction to SCOT Deficiency Mutations in the OXCT1 gene cause SCOT deficiency. The OXCT1 gene […]