Veall R M, Brett E M, Rivinus T M, Stephens R
J Ment Defic Res. 1979 Dec;23(4):231-42. doi: 10.1111/j.1365-2788.1979.tb00858.x.
A new case of the Borjeson-Forssman-Lehmann syndrome is described with details of anthropometry, dermatoglyphs, endocrine function studies and mental state. Comparisons are made with the five previously reported cases. The diagnosis is based on the clinical appearance. Endocrine studies gave normal results and the patient's short stature is not due to growth hormone deficiency. There is no evidence for primary hypogonadism.
本文描述了一例新的博尔杰森-福斯曼-莱曼综合征病例，并详细介绍了人体测量学、皮纹学、内分泌功能研究及精神状态。与之前报道的五例病例进行了比较。诊断基于临床表现。内分泌研究结果正常，患者身材矮小并非由于生长激素缺乏。没有证据表明存在原发性性腺功能减退。
