Bernd L, Martini A K, Schiltenwolf M
Stiftung Orthopädische Universitätsklinik Heidelberg.
Klin Padiatr. 1990 Jan-Feb;202(1):60-3. doi: 10.1055/s-2007-1025488.
The leading symptom of Catel-Manzke syndrome is a characteristic deviation of index fingers. Further the patients suffer from symptoms of Pierre-Robin syndrome (micrognathia, glossoptosis, cleft palate). The survival of patients, mostly male, depends on the severeness of congenital malformation of the face skull. The rare disease is demonstrated and discussed by two own cases.
卡特-曼兹克综合征的主要症状是食指的特征性偏斜。此外,患者还患有皮埃尔-罗宾综合征的症状(小颌畸形、舌后坠、腭裂)。患者(大多为男性)的存活取决于面颅骨先天性畸形的严重程度。通过两例自身病例对这种罕见疾病进行了展示和讨论。