Megalocornea. Clinical and genetic aspects. - Suppr | 超能文献

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Megalocornea. Clinical and genetic aspects.

Doc Ophthalmol. 1994;87(1):1-121. doi: 10.1007/BF01676641.

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Concurrent presentation of aniridia and megalocornea without glaucoma.无青光眼的无虹膜和大角膜同时表现。

J AAPOS. 2011 Jun;15(3):297-8. doi: 10.1016/j.jaapos.2011.02.007. Epub 2011 Jun 12.

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[Congenital megalocornea].[先天性大角膜]

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LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma.常染色体隐性遗传眼病综合征伴大角膜、球形晶状体和继发性青光眼的 LTBP2 基因突变。

Eur J Hum Genet. 2010 Jul;18(7):761-7. doi: 10.1038/ejhg.2010.11. Epub 2010 Feb 24.

5

[Hereditary anterior megalophthalmus--a genealogical study of 12 patients in 4 generations].[遗传性前部巨眼症——对4代人中12例患者的系谱研究]

Klin Monbl Augenheilkd. 2000 Nov;217(5):284-8. doi: 10.1055/s-2000-10369.

6

Megalocornea: a clinical and echographic study of an autosomal dominant pedigree.巨角膜：一个常染色体显性遗传家系的临床及超声检查研究

J Pediatr Ophthalmol Strabismus. 1984 Sep-Oct;21(5):190-3. doi: 10.3928/0191-3913-19840901-08.

7

Anterior megalophthalmos with pigmentary glaucoma.伴有色素性青光眼的前部巨眼症

Graefes Arch Clin Exp Ophthalmol. 2005 Oct;243(10):1066-8. doi: 10.1007/s00417-005-1157-2. Epub 2005 Oct 20.

8

Autosomal-dominant inheritance of megalocornea associated with down's syndrome.与唐氏综合征相关的大角膜的常染色体显性遗传。

Am J Ophthalmol. 1974 Sep;78(3):526-9. doi: 10.1016/0002-9394(74)90245-1.

9

Goniodysgenesis and hereditary juvenile glaucoma. A clinical study of a Swedish pedigree.前房角发育异常与遗传性青少年青光眼。瑞典一个家系的临床研究。

Acta Ophthalmol Suppl. 1970;107:3-100.

10

Megalocornea-mental retardation syndrome.巨角膜-智力发育迟缓综合征

Indian Pediatr. 2005 Aug;42(8):835-6.

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Calculating intraocular lens power in anterior megalophthalmos: A case report.前部巨眼症人工晶状体屈光度的计算：一例报告

Front Med (Lausanne). 2022 Aug 17;9:926792. doi: 10.3389/fmed.2022.926792. eCollection 2022.

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Abnormal corneal properties in osteogenesis imperfecta and glaucoma: a case series.成骨不全症与青光眼患者的角膜异常特性：病例系列研究

BMJ Open Ophthalmol. 2021 Apr 15;6(1):e000684. doi: 10.1136/bmjophth-2020-000684. eCollection 2021.

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Management of cataract in a patient with anterior megalophthalmos.患有先天性大眼球患者的白内障治疗

本文引用的文献

1

[About Ectopia lentis without Arachnodactyly and its Relationship to Ectopia lentis et pupillae].[关于无蜘蛛指（趾）的晶状体异位及其与晶状体异位和瞳孔异位的关系]

Ophthalmologica. 1947 Jul;114(1):16-32. doi: 10.1159/000300446.

2

CONGENITAL MIOSIS OR PINHOLE PUPILS OWING TO DEVELOPMENTAL FAULTS OF THE DILATATOR MUSCLE.先天性瞳孔缩小或针孔样瞳孔，由于瞳孔开大肌发育缺陷所致。

Br J Ophthalmol. 1923 Sep;7(9):401-19. doi: 10.1136/bjo.7.9.401.

3

Marfan's syndrome (arachnodactyly) with arthrogryposis (amyoplasia congenita).伴有关节挛缩（先天性肌发育不全）的马方综合征（蜘蛛指）