{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,17]],"date-time":"2025-10-17T21:40:02Z","timestamp":1760737202582,"version":"build-2065373602"},"reference-count":18,"publisher":"BMJ","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[1980,2]]},"abstract":"<jats:p>A review of published clinical reports shows that anorexia nervosa has been found in association with several genetic anomalies, principally gonosomal aneuploidy. An additional, and unique, association is described here: a case of anorexia nervosa in a patient with the yellow mutant form of oculocutaneous albinism and no other apparent chromosomal abnormalities. While the concurrence of these two disorders in a single person is apparently a chance phenomenon, our review of experimental publications shows that feeding disturbances also occur in yellow mutant mice. Such complementary findings suggest the need for continuing investigation of the genetic foundations of eating behaviour.<\/jats:p>","DOI":"10.1136\/jmg.17.1.68","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T14:52:06Z","timestamp":1226328726000},"page":"68-71","source":"Crossref","is-referenced-by-count":2,"title":["Concurrence of anorexia nervosa and yellow mutant albinism."],"prefix":"10.1136","volume":"17","author":[{"given":"J T","family":"Kelly","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J","family":"Rohde","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"suffix":"Jr","given":"C J","family":"Witkop","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A","family":"Johannes","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1980,2,1]]},"reference":[{"key":"ref_1","first-page":"48","article-title":"and (2) normal karyotype with some chromatid breakage and retardation of leucocyte response to mitogenic (phytohaemagglutinen) stimulation. The unusual genetic condition concurrent with this case of anorexia nervosa is the yellow mutant form of oculocutaneous albinism. This condition causes less photophobia and social reaction than other types of albinism, but may involve subclinical perceptual or visual system anomalies. At present we Hill OW. Epidemiologic aspects of anorexia nervosa","volume":"9","author":"intravenous pyelogram; cytoscopy","year":"1977","unstructured":"intravenous pyelogram, and cytoscopy, and (2) normal karyotype with some chromatid breakage and retardation of leucocyte response to mitogenic (phytohaemagglutinen) stimulation. The unusual genetic condition concurrent with this case of anorexia nervosa is the yellow mutant form of oculocutaneous albinism. This condition causes less photophobia and social reaction than other types of albinism, but may involve subclinical perceptual or visual system anomalies. At present we Hill OW. Epidemiologic aspects of anorexia nervosa. 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