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1. 原発性（先天性）脳ヘルニア primary congenital encephalocele
2. 鼻の先天異常 congenital anomalies of the nose
3. 神経管欠損症の超音波診断 ultrasound diagnosis of neural tube defects
4. 神経管欠損の出生前スクリーニングおよび診断 prenatal screening and diagnosis of neural tube defects
5. キアリ奇形 chiari malformations

A review of Meckel-Gruber syndrome - incidence and outcome in the state of Qatar.

Al-Belushi M1, Al Ibrahim A1, Ahmed M1, Ahmed B1,2, Khenyab N1, Konje JC1,3.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.J Matern Fetal Neonatal Med.2016 Jun;29(12):2013-6. doi: 10.3109/14767058.2015.1072162. Epub 2015 Aug 26.
Meckel-Gruber (MKS) syndrome is a lethal autosomal abnormality diagnosed most commonly from classical findings on ultrasound scan after the late first trimester. There are few reports of cases followed up antenatally until delivery. We report here one of the largest series of 19 cases diagnosed ante
PMID 26333300

Parietal and occipital encephalocele in same child: A rarest variety of double encephalocele.

Sharma S1, Ojha BK2, Chandra A3, Singh SK4, Srivastava C5.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.Eur J Paediatr Neurol.2016 May;20(3):493-6. doi: 10.1016/j.ejpn.2015.12.008. Epub 2016 Feb 4.
An encephalocele is a protrusion of the brain and/or meninges through a defect in the skull. Based on the location of the skull defect they are classified into sincipital, basal, occipital or parietal varieties. Occurrence of more than one Encephalocele in a patient is very rare and very few cases o
PMID 26876766

Sivrikoz TS1, Altunoglu U2, Kalelioglu İH1, Yüksel A1, Uyguner OZ2, Has R1, Kayserili H2,3.
Prenatal diagnosis.Prenat Diagn.2016 Apr 15. doi: 10.1002/pd.4826. [Epub ahead of print]
PMID 27080046

Hypopituitarism in a patient with transsphenoidal cephalocele : longitudinal changes in endocrinological abnormalities

TANIMOTO Keiji,ONDA Saori,SAWAKI Hideaki,HIRAIWA Tetsuya,SANO Hiroyuki,OHNISHI Mineki,TERASAKI Jungo,HANAFUSA Toshiaki
Endocrine journal 58(3), 193-198, 2011-03-01
NAID 10029587911