Maroteaux P, Fonfria M C
Unité de Recherchés de Génétique Médicale (INSERM U12 and CNRS UA 584), Hôpital des Enfants-Malades, Paris, France.
Am J Med Genet. 1987 Sep;28(1):153-8. doi: 10.1002/ajmg.1320280122.
Two patients are described with a syndrome which resembles Apert syndrome with polydactyly of hands and feet. This association is apparently rare and we think that this may represent a distinct syndrome separate from Apert syndrome.
描述了两名患有类似阿佩尔综合征的患者，伴有手足多指畸形。这种关联显然很少见，我们认为这可能代表一种与阿佩尔综合征不同的独特综合征。
