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Chinese Journal of Stomatological Research(Electronic Edition) ›› 2018, Vol. 12 ›› Issue (06): 389-392. doi: 10.3877/cma.j.issn.1674-1366.2018.06.012

Special Issue:

• Case Report • Previous Articles    

Diaphragmatic hernia in a patient with Kabuki syndrome: case report and literature review

Zhizhu Meng1, Qiang Liu1, Xiaofeng Bai1, Zeliang Zhang1, Li Lu1,()   

  1. 1. Department of Oral and Maxillofacial Surgery, Institute of Stomatology, Liaoning Province; Liaoning Province Dental Disease Transformation Medical Research Center; Key Laboratory of Oral Diseases in Liaoning Province; Department of Oral and Maxillofacial Surgery, School Stomatology, China Medical University, Shenyang 110002, China
  • Received:2018-06-13 Online:2018-12-01 Published:2018-12-01
  • Contact: Li Lu
  • About author:
    Corresponding author: Lu Li, Email:

Abstract:

Kabuki syndrome (KMS) is characterized by multiple congenital anomalies with an incidence of 1/32 000 in Japan. There is no any standard of dignosis for KMS. Five diagnostic criteria for KMS are as follows, including a characteristic facial dysmorphism, skeletal anomalies, dermatoglyphic anomalies, postnatal short stature and mild to moderate mental retardation. In addition, other rare clinical features also have implications for the diagnosis of KMS. Congenital diaphragmatic hernia (CDH) is an unfrequent concomitnta symptom in KMS. In this case report, we describe a 12-month-old boy with KMS who is diagnosed with CDH and cleft palate. It is recommended that careful dysmorphological examination should be performed in all patients with KMS. Meanwhile, a prudent anesthetic management is of great importance for such patients.

Key words: Kabuki syndrome, Congenital diaphragmatic hernia, Cleft palate

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