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上颌寄生胎、双垂体及胼胝体发育不全。

Epignathus, double pituitary and agenesis of corpus callosum.

作者信息

Bale P M, Reye R D

出版信息

J Pathol. 1976 Nov;120(3):161-4. doi: 10.1002/path.1711200305.

DOI:10.1002/path.1711200305
PMID:1003267
Abstract

Two infants from unrelated families died on the 1st day of life with epignathus, duplication of the entire pituitary, infundibulum and sella, and widening or separation of midline structures of the head including absent corpus callosum. We suggest that some infants surviving surgery for large epignathi may have relatively symptomless absent corpus callosum or double pituitary.

摘要

来自两个无亲缘关系家庭的两名婴儿在出生第一天死亡,他们患有上颌寄生胎、整个垂体、漏斗和蝶鞍重复,以及头部中线结构增宽或分离,包括胼胝体缺失。我们认为,一些接受大型上颌寄生胎手术存活下来的婴儿可能有无症状的胼胝体缺失或双垂体。

相似文献

1
Epignathus, double pituitary and agenesis of corpus callosum.上颌寄生胎、双垂体及胼胝体发育不全。
J Pathol. 1976 Nov;120(3):161-4. doi: 10.1002/path.1711200305.
2
[Familial agenesis of the corpus callosum: a new form].[家族性胼胝体发育不全:一种新形式]
Arch Fr Pediatr. 1993 Apr;50(4):327-30.
3
Spectrum of corpus callosum agenesis.胼胝体发育不全的谱系
Pediatr Neurol. 2005 Feb;32(2):94-101. doi: 10.1016/j.pediatrneurol.2004.09.007.
4
Agenesis of corpus callosum and anophthalmia in the asplenia syndrome. A recognisable association?无脾综合征中的胼胝体发育不全和无眼畸形。一种可识别的关联?
Ann Genet. 1997;40(1):14-7.
5
[A case of hypopituitarism associated with empty sella and agenesis of corpus callosum, a variant form of septo-optic-pituitary dysplasia].[一例与空蝶鞍及胼胝体发育不全相关的垂体功能减退症,一种视隔-垂体发育异常的变异形式]
Fukuoka Igaku Zasshi. 1990 Dec;81(12):396-401.
6
[Agenesis of the corpus callosum in newborn infants diagnosed by trans-fontanelle echography].
Ned Tijdschr Geneeskd. 1987 Aug 29;131(35):1516-9.
7
Agenesis of the corpus callosum: real-time ultrasonographic diagnosis and autopsy findings.胼胝体发育不全:实时超声诊断与尸检结果
Helv Paediatr Acta. 1985 Dec;40(5):371-80.
8
[Cerebral malformation in the newborn: holoprosencephaly and agenesis of the corpus callosum].新生儿脑畸形:前脑无裂畸形和胼胝体发育不全
Rev Neurol. 2003;36(2):179-84.
9
Agenesis of the corpus callosum, abnormal genitalia and intractable epilepsy due to a novel familial mutation in the Aristaless-related homeobox gene.由于无尾相关同源框基因的一种新型家族突变导致的胼胝体发育不全、生殖器异常和难治性癫痫。
Neuropediatrics. 2004 Jun;35(3):157-60. doi: 10.1055/s-2004-817919.
10
Agenesis of corpus callosum, hypertrophic pyloric stenosis and Hirschsprung disease: coincidence or common etiology?
Neuropediatrics. 1996 Aug;27(4):204-6. doi: 10.1055/s-2007-973789.

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Brain malformations associated with epignathus: a clue for the correct prenatal diagnosis.与颅咽管瘤相关的脑畸形:正确产前诊断的线索。
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Pituitary duplication and nasopharyngeal teratoma in a newborn: CT, MRI, US and correlative histopathological findings.新生儿垂体重复畸形与鼻咽部畸胎瘤:CT、MRI、超声及相关组织病理学表现
Neuroradiology. 2005 Jul;47(7):558-61. doi: 10.1007/s00234-005-1374-8. Epub 2005 Jun 8.
6
Review of the embryologic development of the pituitary gland and report of a case of hypophyseal duplication detected by MRI.垂体胚胎发育回顾及1例经磁共振成像检测到的垂体重复病例报告。
Neuroradiology. 1995 Jan;37(1):3-12. doi: 10.1007/BF00588511.
7
Nasopharyngeal teratoma ('hairy polyp'), Dandy-Walker malformation, diaphragmatic hernia, and other anomalies in a female infant.一名女婴患有鼻咽部畸胎瘤(“毛发样息肉”)、Dandy-Walker畸形、膈疝及其他异常。
J Med Genet. 1990 Dec;27(12):788-90. doi: 10.1136/jmg.27.12.788.