Total: 5 |
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PMID (PMCID) | ||
---|---|---|
21301038 |
MIXED_SAMPLE | Young Adult |
[Satoyoshi syndrome]. | ||
Satoyoshi E. Brain Nerve. 2011;63(2):141-6. |
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Satoyoshi syndrome is a rare disorder of unknown case characterized by progressive painful intermittent muscle spasms, alopecia, malabsorption amenorrhea and skeletal abnormalities mimicking a skeletal dysplasia. | ||
19623421 |
FEMALE | |
[Satoyoshi syndrome: report of one case]. | ||
Castiglioni C, Diaz A, Moenne K, Mericq V, Salvador F, Hernandez C. Rev Med Chil. 2009;137(4):542-6. |
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Satoyoshi syndrome is a rare multisystemic disease of presumed autoimmune etiology characterized by progressive painful intermittent muscle spasms, diarrhea frequently associated with malabsorption, alopecia, skeletal abnormalities and endocrine disorders with a poor long-term prognosis due to early crippling. | ||
18607399 |
FEMALE | Middle Aged |
A case of adult-onset Satoyoshi syndrome with gastric ulceration and eosinophilic enteritis. | ||
Asherson RA, Giampaolo D, Strimling M. Nat Clin Pract Rheumatol. 2008;4(8):439-44. |
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Satoyoshi syndrome with autoimmune features (high levels of antinuclear antibody and antibodies to thyroid tissue) and malabsorption due to eosinophilic enteritis. | ||
12039433 |
MALE | Adult |
A unilateral presentation of 'Satoyoshi syndrome'. | ||
Uddin AB, Walters AS, Ali A, Brannan T. Parkinsonism Relat Disord. 2002;8(3):211-3. |
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Although previous literature had postulated malabsorption and autoimmune mechanism as pathogenic for Satoyoshi syndrome, the presence of a strictly unilateral presentation argues against those hypotheses. | ||
9133353 |
FEMALE | Adult |
Radiological and orthopedic abnormalities in Satoyoshi syndrome. | ||
Haymon M, Willis RB, Ehlayel MS, Lacassie Y. Pediatr Radiol. 1997;27(5):415-8. |
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Satoyoshi syndrome is a rare disorder of unknown etiology characterized by progressive, painful intermittent muscle spasms, severe skeletal abnormalities mimicking a skeletal dysplasia, malabsorption, alopecia, and amenorrhea. |