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Dahlberg Borer Newcomer syndrome; Dandy–Walker syndrome; De Barsy syndrome; de Clérambault's syndrome; De Quervain syndrome; De Winter syndrome; Dead arm syndrome; Deficiency of the interleukin-1–receptor antagonist; Degenerative disc disease; Dejerine–Roussy syndrome; Delayed sleep phase disorder; Delusional misidentification syndrome ...
The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child.
Dandy–Walker syndrome recessive form; Dandy–Walker malformation with mental retardation, basal ganglia disease, and seizures; Dandy–Walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy; Dandy–Walker syndrome; Daneman–Davy–Mancer syndrome; Darier's disease; Davenport–Donlan syndrome; DAVID syndrome
Like many autoimmune diseases, SPS exists on a spectrum and, as a result, symptoms can look quite different in different people, Dr. Scott Newsome, head of the Johns Hopkins Stiff Person Syndrome ...
This is a list of major and frequently observed neurological disorders (e.g., Alzheimer's disease), symptoms (e.g., back pain), signs (e.g., aphasia) and syndromes (e.g., Aicardi syndrome). There is disagreement over the definitions and criteria used to delineate various disorders and whether some of these conditions should be classified as ...
Stiff-person syndrome, aka Moersch-Woltman syndrome, is a neurological disorder that can cause symptoms such as stiffening in the muscles of the trunk, along with stiffness and rigidity in the ...
Celine Dion Courtesy of Celine Dion/Instagram Céline Dion celebrated International Stiff Person Syndrome Day amidst her battle with the disorder by sharing a rare photo of her children. “Today ...
The condition was dubbed "Jones Syndrome" later that year but this term is not widely used as another condition is also known by this name. In 2010, another family of Moroccan-Jewish origin were reported to have the syndrome, and it was noted that the posterior fossa anomalies were most likely responsible for the development of hydrocephalus. [2]