WebObjective To describe the clinical and molecular genetic findings in 2 carriers of Duchenne muscular dystrophy (DMD) who exhibited marked hemiatrophy. Duchenne muscular dystrophy is an X-linked disorder in which affected male patients harbor mutations in the dystrophin gene. Female patients with heterozygous mutations may be manifesting carriers. WebApr 30, 2024 · Other features which occur in some (but not all) patients are: Altered sensation and tingling in the thigh, hip or buttock, which tends to be mild in comparison to the pain and... About half of patients also have distal neuropathy, meaning that sensation … Diabetic neuropathy can cause problems with the sensory, motor and autonomic …
Parry-Romberg syndrome Radiology Reference Article - Radiopaedia
WebEpileptic encephalopathies are conditions in which neurologic deterioration is attributable entirely or partly to epileptic activity. It can be due to very frequent or severe seizures … WebJul 26, 2024 · Hemihyperplasia, formerly called hemihypertrophy, is a rare disorder in which one side of the body grows more than the other due to an excess production of cells, … tshirt animation
Diabetic Amyotrophy - Neurology Blogs
WebFeb 18, 2024 · Hemiconvulsion-hemiplegia epilepsy syndrome (HHE) is a clinical syndrome of infancy or early childhood that is associated with seizures, cerebral hemiatrophy and transient or permanent epilepsy. It refers to the characteristic holohemispheric global atrophy of one hemisphere, that is independent of any vascular … WebFeb 3, 2024 · Hemiparkinsonism-hemiatrophy syndrome (HPHA) is a rare neurological syndrome characterized by unilateral atrophy on one side of the body or brain with slowly progressive hemiparkinsonism [].This clinical syndrome differs from idiopathic Parkinson’s disease (PD) in that it usually occurs in young adults and shows diverse responses to … WebJun 30, 2024 · Unilateral cerebral hemiatrophy with ipsilateral compensatory thickening of adjacent bone and hyperpneumatization of sinuses are seen on CT [6]. MRI also shows similar changes along with parenchymal signal changes due to gliosis and porencephalic cysts [7]. MRI also demonstrates the gray-white matter loss with hyperintensities on T2 … t-shirt anker