Magnelli N C, Therman E
J Med Genet. 1975 Mar;12(1):105-8. doi: 10.1136/jmg.12.1.105.
A severely mentally retarded man displayed the following main symptoms: short stature, microcephaly, antimongoloid slant of palpebral fissures, big ears with hyperplastic helices, imperfect dental enamel, short and webbed neck, short arms, short hands, brachymetaphalangy, short second fingers, broad thumbs, short metatarsal bones, and unusually big first toes. It seems almost certain that the syndrome was caused by a chromosome deletion involving about half of 12p which was present in all of the lymphocytes examined.
身材矮小、小头畸形、睑裂反蒙古样倾斜、耳朵大且耳轮增生、牙釉质发育不全、颈部短且有蹼、手臂短、手部短、掌骨短、第二指短、拇指宽、跖骨短以及第一趾异常大。几乎可以确定,该综合征是由涉及12号染色体短臂约一半区域的染色体缺失引起的,在所检测的所有淋巴细胞中均存在这种缺失。