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Doctor insights on: Sjogren Larsson Syndrome

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What adie syndrome, frey syndrome, and shy-drager syndrome have in common?

What adie syndrome, frey syndrome, and shy-drager syndrome have in common?

What do they have in: They all have abnormalities of autonomics and other nervous sytem problems. ...Read more

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What are frey syndrome, horner's syndrome and shy-drager syndrome?

What are frey syndrome, horner's syndrome and shy-drager syndrome?

What do they have in: They all have abnormalities of autonomics and other nervous sytem problems. ...Read more

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My wife is 42. Recently she has been diagnosed with sjogren's syndrome. What is this?

My wife is 42. Recently she has been diagnosed with sjogren's syndrome. What is this?

Autoimmune disease: The most common symptoms in Sjögren's syndrome are dry eyes and dry mouth because white blood cells get "confused" and attack and destroy glands in the body that make tears, saliva, vaginal secretions, and other secretions.Inflammation in Sjögren's can cause rashes or arthritis, and even liver, kidney or brain disease. Can also cause saliva gland cancer (lymphoma), so getting treated is important. ...Read more

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What is smith lemli opitz syndrome?

What is smith lemli opitz syndrome?

Inherited Condition: 1 / 20, 000- 60, 000 newborns are born w/ this condition which can cause malformations of heart, lungs, kidneys, gut & genitalia. Affected babies often have small head size, fused second & third toes &sometimes extra fingers and toes. There can be learning and behavior problems from mild to approaching autism in severity. Infants may grow more slowly, have weaker muscle tone, & have feeding issues. ...Read more

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What is antiphospolipid syndrome (hughes syndrome)?

What is antiphospolipid syndrome (hughes syndrome)?

Antiphospholipids: An autoimune disorder characterized by antibodies to certain phopholipids that predisposes to clotting problmes and pregnancy complications. A certain percentage will develop into systemic lupus. ...Read more

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Is goldenhar syndrome heritable?

Is goldenhar syndrome heritable?

It is a genetic synd: It is a genetic syndrome. There's a bout a 3% chance the child will pass it on and less than a 1% chance it would occur in a sibling of this child of same parents. ...Read more

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What's evans syndrome?

What's evans syndrome?

Anemia: Evans syndrome is a rare type of anemia in which the body makes antibodies that destroys white blood cells, red blood cells and platelets. ...Read more

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Is frey's syndrome familial?

Is frey's syndrome familial?

No: Frey's syndrome is also called auriculotemporal nerve syndrome. This occurs after damage to this nerve in the face from trauma (birth trauma, gun shot, surgery, etc) and as the nerve "regrows" it goes to the surface rather than to the salivary gland. When a person eats something and salivates, the develop a red, non-itchy rash along the face where the nerve is. It's not familial. ...Read more

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Is sjogren's syndrome linked to fibromylgyia? What the symptoms of sjogrens syndrome?

Is sjogren's syndrome linked to fibromylgyia? What the symptoms of sjogrens syndrome?

Sjogren's sydrome: Sjogrens syndrome is an autoimmune disease. The antibodies cause dry eyes dry mouth with musculoskeletal diseases. You also have depression that also compound the problem. Please see a rheumatologist. Thanks. ...Read more

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Is paraneoplastic syndrome genetic?

Is paraneoplastic syndrome genetic?

No: There is no genetic relationship to the development of a paraneoplastic syndrome. ...Read more

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What is neuromytonia (isaacs syndrome)?

What is neuromytonia (isaacs syndrome)?

Neuromyotonia (NMT): Neuromyotonia (nmt), also known as isaacs' syndrome, is a form of peripheral nerve hyperexcitability that causes spontaneous muscular activity resulting from repetitive motor unit action potentials of peripheral origin. Patients with this disorder usually develop: cramps, muscle twitches, muscle stiffness and spasms. Muscle relaxation can difficult and hand getting stuck closed is one example. ...Read more

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Which person discovered crouzonodermoskeletal syndrome (crouzon syndrome)?

Which person discovered crouzonodermoskeletal syndrome (crouzon syndrome)?

Crouzon: Crouzon craniofacial dysostosis was described by crouzon in 1912. The genetic cause was not identified until 1994 and the credit goes to a number of different geneticists - reardon and preston independently helped narrow the genetic inheritance to the fgfr2 gene. ...Read more

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Is munchausen syndrome herreitery?

Possibly: There may be some hereditary predisposition. Munchausen syndrome was reported in two brothers, two twins and couple families. ...Read more

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Is miller syndrome the same as miller fisher syndrome ?

Is miller syndrome the same as miller fisher syndrome ?

No: Miller Syndrome is a rare condition affecting the face and arms- here is a link with more information http://ghr.nlm.nih.gov/condition/miller-syndrome Miller-Fisher syndrome is causes poor muscle coordination and paralysis of the eye muscles - here is a link for MFS http://www.ninds.nih.gov/disorders/miller_fisher/miller_fisher.htm ...Read more

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Goldenhar syndrome treatment?

Goldenhar syndrome treatment?

Birth defect: Congenital birth defect that affects the development of the ear, nose, mandible, and palate. ...Read more

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What is gillian barre syndrome?

What is gillian barre syndrome?

Autoimmune: An autoimmune disease that attacks the myelin sheaths on your peripheral nerves. Usually starts in feet an ascends. Sometimes starts in the eyes. ...Read more

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What is sjogrens syndrome?

What is sjogrens syndrome?

An autoimmune diseas: Sjögren's is an autoimmune disease where the body "turns against itself" and makes antibodies against the mucous secreting areas of the body- the eyes mouth respiratory and genitourinary it is mostly associated as the dry eyes dry mouth syndrome .Other features may include arthritis and kidney disease. It is vital that you see a rheumatologist to evaluate yourcsymptoms make the correct diagnosis a. ...Read more

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Are miller fisher syndrome and Lyme confondible?

Are miller fisher syndrome and Lyme confondible?

?: Please restate question. I am not sure what you mean by confondible. Lyme disease is a tick borne infection. Miller fisher disease is a rare neurologic disorder. Both can have neurologic symptoms. I hope this helps you. If not please ask again ...Read more

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Is there any doctor with experience of seeing patients with Cowden's syndrome, Bannayan-Riley-Ruvalcaba syndrome, PTEN hamartoma tumour syndrome?

Is there any doctor with experience of seeing patients with Cowden's syndrome, Bannayan-Riley-Ruvalcaba syndrome, PTEN hamartoma tumour syndrome?

Cowden Syndrome: http://ghr.nlm.nih.gov/condition/bannayan-riley-ruvalcaba-syndrome http://ghr.nlm.nih.gov/condition/cowden-syndrome http://rarediseases.info.nih.gov/gard/6202/cowden-syndrome/resources/8 Those are fairly rare disease Perhaps the above links could assist you. Seems like University of Iowa does have expertise. ...Read more