Levin Terry L, Mäkitie Outi, Berdon Walter E, Lachman Ralph S
Division of Pediatric Radiology, Department of Radiology, Montefiore Medical Center, 111 E. 210 St., Bronx, NY, 10467, USA,
Pediatr Radiol. 2015 Jul;45(7):1066-71. doi: 10.1007/s00247-014-3231-6. Epub 2014 Nov 23.
Shwachman-Bodian-Diamond syndrome (OMIM 260400) was identified in 1964 by pediatricians Harry Shwachman, a leader in cystic fibrosis, and Louis K. Diamond, a hematologist, along with pediatrician and morbid anatomist Martin Bodian. Initially the syndrome's clinical presentation included exocrine pancreatic insufficiency (lipomatous replacement of the pancreas) and neutropenia. In 1967 skeletal changes of metaphyseal chondrodysplasia were also described, completing the triad of findings; these abnormalities are present in all affected children and should be viewed as an integral feature of the syndrome, also called Shwachman-Diamond syndrome.
施瓦赫曼-博迪安-戴蒙德综合征(OMIM 260400)于1964年由儿科医生哈利·施瓦赫曼(囊性纤维化领域的领军人物)、血液学家路易斯·K·戴蒙德以及儿科医生兼病理解剖学家马丁·博迪安共同发现。最初,该综合征的临床表现包括外分泌性胰腺功能不全(胰腺脂肪化生)和中性粒细胞减少。1967年,还描述了干骺端软骨发育异常的骨骼变化,从而形成了三联征表现;这些异常存在于所有患病儿童中,应被视为该综合征(也称为施瓦赫曼-戴蒙德综合征)的一个固有特征。