Braddock S R, Lachman R S, Stoppenhagen C C, Carey J C, Ireland M, Moeschler J B, Cunniff C, Graham J M
Ahmanson Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, CA 90048.
Am J Med Genet. 1993 Nov 15;47(7):1006-13. doi: 10.1002/ajmg.1320470714.
Brachmann-de Lange syndrome (BDLS) is a well-delineated disorder consisting variably of pre- and postnatal growth deficiency, microbrachycephaly, characteristic face, hypertrichosis, visceral anomalies, and limb defects consisting primarily of variable limb reduction defects, micromelia, and elbow abnormalities. The course is usually marked by initial hypertonicity, low-pitched weak cry, feeding problems, and behavioral problems with marked mental deficiency. In classical cases there is rarely any difficulty in making the diagnosis, but for mildly affected cases, it may be difficult to feel secure about the diagnosis. In an effort to increase the precision of diagnosis for mildly affected cases, we reviewed roentgenograms in 21 cases of Brachmann-de Lange syndrome, as well as previously published descriptions of the radiological manifestations. Unusual radiologic manifestations were related primarily to the limb anomalies, and these were often asymmetric. These manifestations included digital abnormalities, which ranged from acheiria to oligodactyly, hypoplasia of the thumb and first metacarpal, clinodactyly of the fifth finger, or ectrodactyly. Long bone abnormalities included ulnar a/hypoplasia, dysplasia of the radial head, or fusion of the elbow. When there was a single forearm bone, there was often fusion at the elbow and oligodactyly, which made it difficult to determine whether the radius or ulna was absent. Other radiologic manifestations included 13 ribs with precocious sternal fusion, and micrognathia. We suggest that these radiologic manifestations could increase diagnostic precision in mildly affected cases.
布腊克曼-德朗热综合征(BDLS)是一种明确界定的疾病,其特征包括产前和产后生长发育迟缓、小头短头畸形、特殊面容、多毛症、内脏异常以及肢体缺陷,主要表现为各种肢体短小缺陷、短肢畸形和肘部异常。病程通常以最初的肌张力亢进、低音调哭声微弱、喂养问题以及伴有明显智力缺陷的行为问题为特征。在典型病例中,诊断很少有困难,但对于症状较轻的病例,可能难以确定诊断。为了提高对症状较轻病例的诊断准确性,我们回顾了21例布腊克曼-德朗热综合征患者的X线片以及先前发表的有关放射学表现的描述。不寻常的放射学表现主要与肢体异常有关,且通常不对称。这些表现包括手指异常,从无手畸形到多指畸形不等,拇指和第一掌骨发育不全,第五指弯曲畸形或裂手畸形。长骨异常包括尺骨发育不全或发育异常、桡骨头发育异常或肘部融合。当只有一根前臂骨时,肘部常融合且多指畸形,这使得难以确定是桡骨还是尺骨缺失。其他放射学表现包括13根肋骨伴胸骨过早融合以及小颌畸形。我们认为这些放射学表现可提高对症状较轻病例的诊断准确性。