So Wilson, Donahoe Shannon L, Podadera Juan M, Mazrier Hamutal
Sydney School of Veterinary Science, Faculty of Science, The University of Sydney, Sydney, NSW 2006, Australia.
Animals (Basel). 2023 Jun 24;13(13):2091. doi: 10.3390/ani13132091.
Developmental anomalies are an important cause of stillbirth and early perinatal death in companion animals. Many of these disorders remain poorly understood and provide an opportunity as a spontaneous animal model for human disease. Pentalogy of Cantrell is a rare congenital syndrome described in human neonates. It is a ventral midline closure defect with a proposed familial inheritance in humans. This syndrome involves five defects, including the thoracoabdominal wall, sternal, diaphragmatic, pericardial and cardiac malformations. Diverse expressions of these defects have been described in humans and sporadically in domestic animals. This severe syndrome commonly harbors a poor prognosis, posing an ethical and surgical dilemma. To better understand this syndrome and its presentation in dogs, we describe two rare cases of Pentalogy of Cantrell in a litter of papillon dogs. The affected puppies had anomalies compatible with the Pentalogy of Cantrell, including thoracoabdominal schisis, ectopia cordis, sternal cleft, pericardial agenesis, and diaphragmatic defects. The diagnosis was confirmed by advanced imaging (computed tomography) and postmortem examinations. The family history of this litter was explored and other cases in domestic animals were reviewed. This is the first report of the complete Pentalogy of Cantrell with ectopia cordis in the dog and the only report on papillons. Similar to human cases, possible familial inheritance and suspected male gender bias were observed. Further research on this novel animal model, its pathogenesis and its hereditary basis, may be helpful in better understanding this rare developmental disorder.
发育异常是伴侣动物死产和早期围产期死亡的重要原因。其中许多疾病仍未得到充分了解,为人类疾病提供了一个自发的动物模型。坎特雷尔五联症是一种在人类新生儿中描述的罕见先天性综合征。它是一种腹侧中线闭合缺陷,在人类中具有家族遗传倾向。该综合征涉及五个缺陷,包括胸腹壁、胸骨、膈肌、心包和心脏畸形。这些缺陷在人类中已有多种表现,在家畜中也有零星报道。这种严重的综合征通常预后不良,带来了伦理和手术方面的两难困境。为了更好地了解这种综合征及其在犬类中的表现,我们描述了一窝蝴蝶犬中两例罕见的坎特雷尔五联症病例。患病幼犬具有与坎特雷尔五联症相符的异常,包括胸腹壁裂、心脏异位、胸骨裂、心包缺如和膈肌缺陷。通过先进的影像学检查(计算机断层扫描)和尸检确诊。我们探究了这窝犬的家族史,并回顾了家畜中的其他病例。这是犬类中首例伴有心脏异位的完整坎特雷尔五联症报告,也是关于蝴蝶犬的唯一报告。与人类病例相似,观察到了可能的家族遗传和疑似的雄性性别偏向。对这种新型动物模型、其发病机制及其遗传基础的进一步研究,可能有助于更好地理解这种罕见的发育障碍。