Kalantar-Hormozi Hadis, Abbaszadeh-Kasbi Ali, Sharifi Guive, Davai Nazanin Rita, Kalantar-Hormozi Abdoljalil
Neuroimaging and Analysis Group of Medical Imaging Center, Imam Khomeini Hospital.
School of Medicine, Tehran University of Medical Sciences (TUMS).
J Craniofac Surg. 2019 Sep;30(6):e514-e517. doi: 10.1097/SCS.0000000000005419.
Craniosynostosis has an incidence of 1 in 2000 to 2500 live births, and is categorized into syndromic and nonsyndromic types. Nonsyndromic ones can be familial in which more than one of the family members are involved.
This is a prospective study which is carried out from April 2015 to January 2018 in 2 academic hospitals. Those patients who had nonsyndromic craniosynostosis and completed medical follow-up were included in the study as well as their 1st degree relatives. Age of patients, gender, existing consanguineous marriage, type of deliveries, type of pregnancy (assisted reproductive technologies [ART] versus sexual intercourse), severity and type of craniosynostosis were gathered.
Ninety-four (46.0%), 58 (28.4%), 28 (13.7%), 16 (7.8%), and 8 (3.9%) of patients had trigonocephaly, scaphocephaly, anterior plagiocephaly, complex, and brachycephaly, respectively. A total number of 204 patients were included in the study. Of all 204 families which were included, 30 (14.7%) families had positive familial history. Familial patients were determined in 10, 15, 8, 1, and 5 patients with scaphocephaly, trigonocephaly, anterior plagiocephaly, rachycephaly, and mixed type. Male to female ratio was 2:1, 1.9:1, 1.3:1, 1:1, and 1:1 for scaphocephaly, trigonocephaly, anterior plagiocephaly, brachycephaly, and mixed craniosynostosis. Twelve (5.9%) women had applied ART.
Present study reveals that metopic suture is the most frequent craniosynostosis within nonsyndromic types. All the types of nonsyndromic craniosynostosis had male prevalence but for complex one which was equal in both gender. Nonsyndromic craniosynostosis in about 14.7% of patients was familial.
颅缝早闭在活产婴儿中的发病率为1/2000至1/2500,分为综合征型和非综合征型。非综合征型可能具有家族性,即家族中不止一名成员患病。
这是一项前瞻性研究,于2015年4月至2018年1月在两家学术医院开展。纳入研究的对象为患有非综合征型颅缝早闭且完成医学随访的患者及其一级亲属。收集患者的年龄、性别、是否存在近亲结婚、分娩类型、妊娠类型(辅助生殖技术[ART]与性交)、颅缝早闭的严重程度和类型。
分别有94例(46.0%)、58例(28.4%)、28例(13.7%)、16例(7.8%)和8例(3.9%)患者患有三角头畸形、舟状头畸形、前斜头畸形、复杂型和短头畸形。本研究共纳入204例患者。在纳入研究的所有204个家庭中,30个(14.7%)家庭有阳性家族史。在患有舟状头畸形、三角头畸形、前斜头畸形、短头畸形和混合型的患者中,分别有10例、15例、8例、1例和5例为家族性患者。舟状头畸形、三角头畸形、前斜头畸形、短头畸形和混合型颅缝早闭的男女比例分别为2:1、1.9:1、1.3:1、1:1和1:1。12名(5.9%)女性采用了辅助生殖技术。
本研究表明,在非综合征型颅缝早闭中,额缝早闭最为常见。所有类型的非综合征型颅缝早闭男性患病率均较高,但复杂型在男女中患病率相当。约14.7%的患者非综合征型颅缝早闭具有家族性。