Articles Related to atrophy
Spinal Muscular Atrophy-Type1, Unraveling the tapestry from highly inbred region of North India
spinal muscular atrophy is an autosomal recessive disorder characterized by degeneration of alpha motor in anterior horn
cells of brain and spinal cord, which results in muscular atrophy, hypotonia, fasciculations, areflexia, paralysis and even
death in most severe cases. The underlying cause of this disease is biallelic loss of survival motor neuron 1 (SMN1) gene. Depending upon the clinical features & patient's age, SMA is classified into different distinctive sub types
A Novel Coenzyme Q8A Mutation in a Case with Juvenile-Onset Coenzyme Q10D4: Case Report and Literature Review
Primary coenzyme Q10 deficiency-4 (CoQ10D4) is an autosomal recessive disorder characterized by childhood-onset of cerebellar ataxia and exercise intolerance. Molecular pathology responsible for clinical findings is mitochondrial respiratory chain dysfunction. The main clinical manifestation involves early-onset exercise intolerance, progressive
cerebellar ataxia and movement disorders. Some affected individuals develop seizures and have mild mental impairment, indicating variable severity.
Two Approaches in the Cosmetic Reabilitation of Patients with Post-Traumatic Subatrophy of the Eyeball
To define groups of patients who may hold prosthetics subatrophic eyes and removes the eye with subsequent prosthetics. Under observation from 2010-2017 was 152 patients with posttraumatic subatrophy (the average age is 46.1 years), divided into 2 groups: 1-102(67,1%) patient who underwent enucleation with the for-mation of the locomotor stump - 56 (55,0%), evisceration - 46 (45,0%); and group 2 - 50 (32.9%) and patients who have had prosthetic subatrophic eyes.
Hyperkinetic Manifestation in a Patient with Hippocampal Atrophy
Describes a case of a patient that presents with hippocampal atrophy leading to hyperkinetic crises of parietal-occipital origin
Parry Romberg Syndrome: A Case Report
Parry-Romberg syndrome is a rare disorder characterized by slowly progressive deterioration of the skin and soft tissues of half of the face. The syndrome presents with characteristic skeletal, dental, and soft tissue changes in the affected half of the face, with or without neurological signs and symptoms.
Case Studies of 17 Patients
This retrospective review of 17 patients suggests an increased risk of adverse events including premature death with opiate discontinuation long after withdrawal stage. The results are consistent with previously reported yet not fully understood – opiate associated neuro protective mechanism – against premature death for some vulnerable subgroups.
A Highly Efficient Culture Technique for Derivation of Motor Neurons from Human Umbilical Cord Derived Mesenchymal Stem Cells
Motor Neuron Diseases (MND) are a group of progressive neurological disorders that destroy motor neurons, cells that control essential muscle activity. Despite the advances in treatment modalities, the overall survival rate has not changed for decades. This is mainly due to the lack of effective methods.
Unusual Variant of Guillain-Barré Syndrome Following Hepato-biliary Surgery — A Rare Case Report
Guillain-barré syndrome (G.B. Syndrome) is an acute inflammatory poly-radiculoneuropathy characterized by weakness and areflexia typically following viral infection, vaccination, and rarely surgery. Acute Inflammatory Demyelinating Poly-radiculoneuropathy is the most common subtype of G.B. Syndrome. Although post-operative G.B. syndrome is a rare entity, there are few case reports of G.B. syndrome after gastric surgery. But there have been no reported case scenarios of atypical variety of this neurologic entity following hepato billiary surgery. Hence our objective is to put forward this message to the readers.
Dermatophytosis in a Dog Seropositive for Ehrlichia Spp
In this report, we present a case of dermatophytosis in a dog seropositive for Ehrlichia spp.Mild annular skin lesions observed on initial presentation persisted and became worse during the course of antibiotic therapy. Microscopic examination of the fungal culture of skin scrapings revealed infection with Microsporum gypseum. The patient fully recovered following treatment with topical 1% clotrimazole and antifungal shampoo.
Does Physical Activity and Sport Practice Lead to a Healthier Lifestyle and Eating Habits in Male Adolescents?
The prevalence of childhood obesity has been increasing rapidly and there is general consensus that good nutritional practices and physical activity should be encouraged as early as possible in life. The aim of this study was to describe and to compare the current lifestyle and dietary pattern of normal weight (NW) and overweight + obese (OW+OB) male adolescents who are physically active.
MAPK Pathway in Skeletal Muscle Diseases
Mitogen-Activated Protein Kinase (MAPK) pathway is a signal transduction pathway that functions in a wide range of physiological and pathophysiological cellular events including cell proliferation, differentiation, apoptosis, migration, inflammation, metabolic disorders and diseases.
Editorial Board Members Related to atrophy
Subash Sad
Professor
Department of Biochemistry, Microbiology and Immunology
University of Ottawa
Canada
Department of Biochemistry, Microbiology and Immunology
University of Ottawa
Canada
Jean-François Desaphy
Associate Professor
Department of Pharmacy & Drug Sciences
University of Bari
Italy
Department of Pharmacy & Drug Sciences
University of Bari
Italy