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Temple syndrome is a rare genetic disorder that is caused by mutations in paternal chromosome 14 or by maternal UPD(14). [2] The signs of this syndrome are oligohydramnios, intrauterine growth restriction, small placenta, low birth weight and length, hypotonia, motor and speech delay, joint laxity, clinodactyly, kyphoscoliosis, precocious puberty, obesity and the facial signs are ...
There are several viral infections that can affect the throat and uvula, many of which also cause cold symptoms (runny nose, cough, laryngitis). “Some viruses, like coxsackie (hand, foot, and ...
As hyaluronidase deficiency is an extremely rare disorder, a clear clinical picture of the disease has not been formed. However, the following symptoms may occur: [2] ...
Different versions of the ICD code exist worldwide. The United States currently uses the ICD-10-CM, a Clinical Modification of the World Health Organization standard for diagnoses adapted for insurance reimbursement and billing purposes. This version allows for further breakdown of a code, which increases diagnosis specificity.
The disease course, anatomy, and laterality can vary widely and are important to consider in diagnosis and treatment. Cases may be acute (sudden onset with < 3 month duration) and monophonic, acute and recurrent, or chronic. [13] The signs and symptoms of uveitis may include the following: [1]
Correctly classifying the Castleman disease subtype is important, as the three subtypes vary significantly in symptoms, clinical findings, disease mechanism, treatment approach, and prognosis. All forms involve overproduction of cytokines and other inflammatory proteins by the body's immune system as well as characteristic abnormal lymph node ...
During the late 1990s and the 2000s, researchers (including Finkelstein, [4] Schmidt, Larrosa [5] and others) published data which questioned the efficiency of the treatment and demonstrated that in a considerable number of cases, laser-assisted uvulopalatoplasty may also cause mild obstructive sleep apnea in patients who has been nonapneic ...
Epilepsy symptoms could begin with light anxiety attacks and can be controlled with anti-epileptic medications. [10] Other patients present with symptoms similar to schizophrenia while some suffer from mood, anxiety, and psychotic disorders. [16] [19] Chromosome 1, where the ECM1 mutation occurs at 1q21