Bennett C P, Berry A C, Maxwell D J, Seller M J
Division of Medical and Molecular Genetics, Guy's Hospital, London, UK.
Am J Med Genet. 1992 Dec 1;44(6):795-9. doi: 10.1002/ajmg.1320440615.
A 22-week fetus who had died in utero had a markedly hypoplastic nose and other facial abnormalities, short fingers, hypoplastic nails, and small phallus. Radiologically there was symmetrical cartilaginous stippling of the vertebral column, femoral heads, calcanei and elbows typical of chondrodysplasia punctata (CP), and metacarpal shortness and tiny pyramidal phalanges. The several causally different forms of CP are tabulated. Differential diagnosis suggests that the present case, which does not have limb shortness, could be a case of X-linked recessive brachytelephalangic chondrodysplasia punctata.
一名在子宫内死亡的22周胎儿有明显发育不全的鼻子和其他面部异常、短指、发育不全的指甲以及小阴茎。放射学检查显示,脊柱、股骨头、跟骨和肘部有对称性软骨点状钙化,这是点状软骨发育异常(CP)的典型表现,同时还有掌骨短小和微小的锥形指骨。文中列出了几种病因不同的CP类型。鉴别诊断表明,本病例没有肢体短小的情况,可能是X连锁隐性短指型点状软骨发育异常。