Satoyoshi syndrome

Satoyoshi syndrome is a rare, multisystemic autoimmune disease mainly characterized by intermittent painful muscle spasms, alopecia (totalis or universalis in most cases) and long-lasting diarrhea that could lead to malnutrition, growth retardation, and amenorrhea. Secondary bone deformities and various endocrine anomalies may also be associated. Antinuclear antibodies are reported in many cases.

Skeletal dysplasia

A general term describing features characterized by abnormal development of bones and connective tissues.


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PMID (PMCID)
21301038
 MIXED_SAMPLE Young Adult
[Satoyoshi syndrome].
Satoyoshi E.
Brain Nerve. 2011;63(2):141-6.
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.
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.
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.