Marshall's syndrome or PFAPA (periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis) syndrome is a recently described pediatric periodic disease characterized by recurrent febrile episodes associated with head and neck symptoms. The origin of this syndrome is unknown, and it can last for several years. During healthy periods, patients grow normally. The differential diagnosis includes other diseases characterized by periodic fevers, such as familial Mediterranean fever, familial Hibernian fever, hyperglobulinemia D syndrome, Behçet's disease, cyclic neutropenia, juvenile rheumatoid arthritis, and several Infectious Diseases. Many treatments have been used, with various results, including antibiotics, nonsteroidal anti-inflammatory drugs, acetylsalicylic acid, colchicine, antiviral medicines, steroids, cimetidine, and tonsillectomy. We describe 5 new patients affected by PFAPA syndrome who were observed at the Department of Pediatric Otorhinolaryngology, Spedali Civili, Brescia, Italy, from November 2000 to August 2001. All children underwent physical examination, bacterial, fungal, and viral cultures, chest radiography, and several laboratory studies. The patients were treated by successful tonsillectomy, and after a mean follow-up of 10 months, no recurrence was observed. An analysis of the literature is also presented with particular emphasis on the differential diagnosis of this rare illness and the results of the different therapeutic options.
Sofi Marshall's birth name is Sofia Marshall.
The phone number of the Marshall is: 507-537-7003.
Donyell Marshall's birth name is Donyell Lamar Marshall.
Oswald Marshall's birth name is Robert Oswald Marshall.
Marshall Wayne died in 1999.
Marshall syndrome is a rare genetic disorder, with a prevalence that is not well documented in the general population. It is estimated to occur in fewer than 1 in 100,000 individuals. This means that less than 0.001% of the population is affected by Marshall syndrome.
No it is not yet curable. But there are treatments for it.
Hunters syndrome is a rare genetic disorder that happens when an enzyme malfunctions or is missing completely. Unfortunately, there is no cure for Hunter's syndrome at this time. There are some treatments that can help minimize the symptoms. These treatments include enzyme therapy, gene therapy, and bone marrow transplant.
acetaminophen and antihistamine (diphenhydramine).
There are none.
Marshall syndrome was first described in 1971 by Dr. John Marshall and his colleagues. It is a rare genetic disorder characterized by various features, including distinctive facial traits, skeletal abnormalities, and hearing loss. The syndrome is caused by mutations in the B4GALT7 gene, which affects glycosylation processes in the body.
No, there's no cure, but there are treatments to control the symptoms.
to take him completely & entirely off of your ipod
yes thier is
No, un-fortunately there are not. My cousin has it, he is 19.
I have TAR Syndrome and I asked my doctor if there's any treatments or a cure for it and he said that I would have to have surgery on my arms and they would have to straighten my arms because my arms are bent. I don't know about the blood platelet though.
At the moment, there is no cure for irritable bowel syndrome. However, there are treatments such as taking supplements or medication to decrease diarrhea and other symptoms.