Conditions that can be Mistaken as Early Childhood Glaucoma

被引：22

作者：

Khan, Arif O. ^{[1
]}

机构：

[1] King Khalid Eye Specialist Hosp, Riyadh 11462, Saudi Arabia

来源：

OPHTHALMIC GENETICS | 2011年 / 32卷 / 03期

关键词：

pediatric glaucoma; primary congenital glaucoma; buphthalmos; congenital hereditary endothelial dystrophy; infantile glaucoma; developmental glaucoma; POSTERIOR POLYMORPHOUS DYSTROPHY; INTRAOCULAR-PRESSURE MEASUREMENT; PRIMARY CONGENITAL GLAUCOMA; CENTRAL CORNEAL THICKNESS; X-LINKED MEGALOCORNEA; OF-THE-LITERATURE; PERIVENTRICULAR LEUKOMALACIA; PAPILLORENAL SYNDROME; CLINICAL-FEATURES; CHILDREN;

D O I：

10.3109/13816810.2010.544363

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Primary congenital glaucoma (isolated goniodysgenesis) has classic phenotypic features such as increased measured intraocular pressure, globe enlargement (buphthalmos) with associated myopia, Descemet membrane tears, corneal haze/scarring with associated astigmatism, iris atrophy, and optic nerve cupping. These signs also occur in developmental glaucoma (anterior segment dysgeneses) with infantile onset. However, similar findings can occur in other pediatric conditions which are sometimes are mistaken as early childhood glaucoma.

引用

页码：129 / 137

页数：9

共 39 条

[1] Deleterious mutations in the zinc-finger 469 gene cause brittle cornea syndrome [J].

Abu, Almogit ;

Frydman, Moshe ;

Marek, Dina ;

Pras, Eran ;

Nir, Uri ;

Reznik-Wolf, Haike ;

Pras, Elon .

AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (05) :1217-1222

[2]

Al-Amry M, 2007, J PEDIAT OPHTH STRAB, V44, P192

[3] Retinal detachment and congenital glaucoma [J].

Al-Harthi, Essam ;

Al-Shahwan, Sam ;

Al-Turkmani, Shahira ;

Khan, Arif O. .

OPHTHALMOLOGY, 2007, 114 (08) :1590-1591

[4] Brittle cornea syndrome and its delineation from the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VI): Report on 23 patients and review of the literature [J].

Al-Hussain, H ;

Zeisberger, SM ;

Huber, PR ;

Giunta, C ;

Steinmann, B .

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 124A (01) :28-34

[5] Linkage of Posterior Amorphous Corneal Dystrophy to Chromosome 12q21.33 and Exclusion of Coding Region Mutations in KERA, LUM, DCN, and EPYC [J].

Aldave, Anthony J. ;

Rosenwasser, George O. D. ;

Yellore, Vivek S. ;

Papp, Jeanette C. ;

Sobel, Eric M. ;

Pham, Michele N. ;

Chen, Michael C. ;

Dandekar, Sugandha ;

Sripracha, Ram ;

Rayner, Sylvia A. ;

Sassani, Joseph W. ;

Gorin, Michael B. .

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2010, 51 (08) :4006-4012

[6] Null Mutations in LTBP2 Cause Primary Congenital Glaucoma [J].

Ali, Manir ;

McKibbin, Martin ;

Booth, Adam ;

Parry, David A. ;

Jain, Payal ;

Riazuddin, S. Amer ;

Hejtmancik, J. Fielding ;

Khan, Shaheen N. ;

Firasat, Sabika ;

Shires, Mike ;

Gilmour, David F. ;

Towns, Katherine ;

Murphy, Anna-Louise ;

Azmanov, Dimitar ;

Tournev, Ivailo ;

Cherninkova, Sylvia ;

Jafri, Hussain ;

Raashid, Yasmin ;

Toomes, Carmel ;

Craig, Jamie ;

Mackey, David A. ;

Kalaydjieva, Luba ;

Riazuddin, Sheikh ;

Inglehearn, Chris F. .

AMERICAN JOURNAL OF HUMAN GENETICS, 2009, 84 (05) :664-671

[7] Mucopolysaccharidoses and the eye [J].

Ashworth, JL ;

Biswas, S ;

Wraith, E ;

Lloyd, IC .

SURVEY OF OPHTHALMOLOGY, 2006, 51 (01) :1-17

[8]

Brodsky MC, 2001, ARCH OPHTHALMOL-CHIC, V119, P626

[9]

CAMERON JA, 1991, OPHTHALMOLOGY, V98, P446

[10] Assessment of true intraocular pressure: The gap between theory and practical data [J].

Chihara, Etsuo .

SURVEY OF OPHTHALMOLOGY, 2008, 53 (03) :203-218

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