Asymmetric crying facies and vocal cord paralysis accompanied by congenital heart disease in an infant / 中国当代儿科杂志
Chinese Journal of Contemporary Pediatrics
; (12): 585-588, 2019.
Article
ي Zh
| WPRIM
| ID: wpr-774029
المكتبة المسؤولة:
WPRO
ABSTRACT
A female infant was admitted to the hospital due to perioral cyanosis two hours after birth. The infant was born at the gestational age of 35 weeks by cesarean section with a birth weight of 2 400 g. Physical examination revealed wry mouth to the left side while crying, small auricles, and high palatal arch; fibrolaryngoscopy suggested bilateral vocal cord paralysis; echocardiography suggested ventricular septal defect; single nucleotide polymorphism testing showed 22q11.21 microdeletion. Therefore, the infant was given a definite diagnosis of asymmetric crying facies syndrome accompanied by 22q11.21 microdeletion. After 8-month follow-up, the infant still had asymmetric crying facies with presence of growth retardation.
النص الكامل:
1
الفهرس:
WPRIM
الموضوع الرئيسي:
Cesarean Section
/
Vocal Cord Paralysis
/
Crying
/
Facial Paralysis
/
Heart Defects, Congenital
المحددات:
Female
/
Humans
/
Infant
/
Pregnancy
اللغة:
Zh
مجلة:
Chinese Journal of Contemporary Pediatrics
السنة:
2019
نوع:
Article