OBJECTIVES To define a new type of dominant myotonic muscle disorder and to identify the gene lesion. DESIGN Case series, clinical examination and electromyography, measurements of grip force and relaxation time, and DNA analysis to probe for mutation in the gene for the skeletal muscle sodium channel. SETTING Outpatient clinic and home. PATIENTS Three families studied; all together, 17 a...

AbstractFever is a symptom of illness that commonly found in the Minangkabau ethnic community. This way, community has local knowledge utilizing plants to cure fever. The purpose this study was obtain species used by treatment diseases with symptoms fever, as well their potential modern medicinal ingredients. research method carried out using open, semi-structural, and participatory observation...

Diabetes mellitus is an endocrinological disorder arising from insulin deficiency or due to ineffectiveness of the insulin produced by the body. This results in high blood glucose and with time, to neurological, cardiovascular, retinal and renal complications. It is a debilitating disease and affects the population of every country of the world. Around 200 million people of the world suffer fro...

Memory is the ability of an individual to record the information and recall it whenever needed. Dementia is a mental disorder characterized by loss of intellectual ability (judgment or abstract thinking) which invariably involves impairment of memory. The most common cause of dementia is Alzheimers disease (AD), which is a progressive neurodegenerative disorder associated with loss of neurons i...

One new species named Goeldichironomus adhaerens sp. n. is described from urban area in Manaus, Brazilian Amazon, based on male adult, pupa and larva. New records of G. neopictus Trivinho-Strixino & Strixino, G. maculatus Trivinho-Strixino & Strixino, G. pictus Reiss and G. fluctuans Reiss are also provided.

We describe the case of a girl with a probable autosomal recessive form of nondystrophic hereditary myotonia whose clinical findings are more compatible with the dominant ones mainly myotonia congenita of Thomsen or myotonia fluctuans. Besides the clinical aspects of the atypical form presented by our patient, the efficacy of the more available drugs employed for the treatment of myotonia conge...

Sarcocystis neurona was isolated from the brain of a juvenile, male southern sea otter (Enhydra lutris nereis) suffering from CNS disease. Schizonts and merozoites in tissue sections of the otter's brain reacted with anti-S. neurona antiserum immunohistochemically. Development in cell culture was by endopolyogeny and mature schizonts were first observed at 3 days postinoculation. PCR of merozoi...

During April 2004, 40 sick and dead southern sea otters (Enhydra lutris nereis) were recovered over 18km of coastline near Morro Bay, California. This event represented the single largest monthly spike in mortality ever recorded during 30 years of southern sea otter stranding data collection. Because of the point-source nature of the event and clinical signs consistent with severe, acute neurol...

Sea otters (Enhydra lutris) have been reported to become infected with Toxoplasma gondii and at times succumb to clinical disease. Here, we determined genotypes of 39 T. gondii isolates from 37 sea otters in two geographically distant locations (25 from California and 12 from Washington). Six genotypes were identified using 10 PCR-RFLP genetic markers including SAG1, SAG2, SAG3, BTUB, GRA6, c22...

Gene transcription analysis for diagnosing or monitoring wildlife health requires the ability to distinguish pathophysiological change from natural variation. Herein, we describe methodology for the development of quantitative real-time polymerase chain reaction (qPCR) assays to measure differential transcript levels of multiple immune function genes in the sea otter (Enhydra lutris); sea otter...