Dementia
From Wikidata Jump to navigation Jump to search long-term brain disorders causing personality changes and impaired memory, reasoning, and normal function senility Dementia rare dementia edit English dementia long-term brain disorders causing personality changes and impaired memory, reasoning, and normal function[…][wikidata.org]
Endocrine Dysfunction
Symptoms include dulled facial expressions, hoarse voice, slow speech, eyelids droop, puffy and swollen face and eyes, weight gain, constipation, inability to tolerate cold[brainaacn.org]
Myxedema
The patient loses facial expression, and an appearance of imbecility is quickly observed.[henriettes-herb.com]
He is stupid, inactive, dull of comprehension , is difficult to interest in the surroundings, or he takes an interest in very childish things.[henriettes-herb.com]
Parkinson's Disease
Abstract We present the case of a 78-year-old male who, 16 years ago, was diagnosed with Parkinson's disease (PD) by a neurologist. He initially presented with left-hand tremor, stooped posture, shuffling gait, and frequent falls, which eventually progressed to bilateral motor symptoms after 3 years. Since 2012, his[…][ncbi.nlm.nih.gov]
Parkinsonian Disorder
OBJECTIVE: To provide a 16-year update from the authors' 1996 report documenting a 38% conversion from idiopathic rapid eye movement sleep behavior disorder (iRBD) to a parkinsonian disorder at a mean interval of nearly 13 years after the onset of iRBD in a series of 29 males or 50 years old. METHODS: The[…][ncbi.nlm.nih.gov]
Myotonic Dystrophy
A primiparous pregnant woman in remission of myositis suffered very acute-onset ritodrine-induced rhabdomyolysis. At 29 gestational weeks, ritodrine was administered for threatened preterm labor. Just 3 h later, she complained of severe limb muscle pain, with serum creatinine phosphokinase elevated to 32 019 U/L[…][ncbi.nlm.nih.gov]
Allergic Rhinitis
Abstract Klippel-Feil syndrome KFS, a triad of short neck, limitation of neck movement and low posterior hairline, is characterized by presence of congenitally fused cervical vertebrae and is often associated with multiple congenital anomalies. A 35-year-old male was referred for evaluation of an opaque hemithorax.[…][ncbi.nlm.nih.gov]
Parkinson's Disease Type 3
Parkinson's disease type 3 (PD3) is a form of Parkinson's disease that is inherited in an autosomal dominant manner. The underlying mutation has not yet been identified, but PD3 has been related to a 2.5 Mb-locus on the short arm of chromosome 2. To date, PD3 has been diagnosed in distinct families in Europe and[…][symptoma.com]
Mental Retardation
BACKGROUND, METHODS AND OBJECTIVES: Maternal autoantibodies to neuronal proteins may be one cause of neurodevelopmental disorders. This exploratory study used the Danish archived midgestational sera and their nationwide registers to search for antibodies to the N-methyl-D-aspartate receptor (NMDAR) and[…][ncbi.nlm.nih.gov]
Juvenile Myxedema
Jean L. Bolognia, Joseph L. Jorizzo, Julie V. Schaffer Elsevier Health Sciences, ٠٨/٠٦/٢٠١٢ - 2776 من الصفحات Dermatology, edited by world authorities Jean L. Bolognia, MD, Joseph L. Jorizzo, MD, and Julie V. Schaffer, MD, is an all-encompassing medical reference book that puts the latest practices in dermatologic[…][books.google.com]