Imaizumi K, Ishii T, Masuno M, Kuroki Y
Division of Medical Genetics, Kanagawa Children's Medical Center, Japan.
Clin Dysmorphol. 1998 Jul;7(3):213-6. doi: 10.1097/00019605-199807000-00011.
We describe a male patient with holoprosencephaly, ectrodactyly, cleft lip/cleft palate and hypertelorism. This rare association has previously been reported in two patients. We present a third case and propose a new association representing a distinguishable entity.
我们描述了一名患有前脑无裂畸形、缺指（趾）畸形、唇腭裂和眼距过宽的男性患者。这种罕见的综合征先前在两名患者中已有报道。我们现报告第三例病例，并提出一种新的综合征，代表一种可区分的疾病实体。
