Literature DB >> 8411053

Classification of microphthalmos and coloboma.

M Warburg1.   

Abstract

A new classification of microphthalmos and coloboma is proposed to bring order to the complexity of clinical and aetiological heterogeneity of these conditions. A phenotypic classification is presented which may help the clinician to give a systematic description of the anomalies. The phenotype does not predict the aetiology but a systematic description of ocular and systemic anomalies improves syndrome identification. There are two major classes, total and partial microphthalmos, and a subclassification which follows the embryology of the anomalies. The aetiological classification consists of three classes: (1) genetic (monogenic and chromosomal), (2) prenatally acquired (teratological agents and intrauterine deformations), and (3) associations. Genetic disorders give rise to malformations; prenatally acquired anomalies are disruptions or deformations. The aetiological classification can be applied to other congenital birth defects and improves counselling of families. Recurrence risks vary considerably between the classes.

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Mesh:

Year:  1993        PMID: 8411053      PMCID: PMC1016495          DOI: 10.1136/jmg.30.8.664

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  65 in total

1.  The spectrum of clinical features in CHARGE syndrome.

Authors:  S L Davenport; M A Hefner; J A Mitchell
Journal:  Clin Genet       Date:  1986-04       Impact factor: 4.438

2.  Bilateral microphthalmos with orbital cysts: MR findings.

Authors:  D C Wright; W T Yuh; H S Thompson; J A Nerad
Journal:  J Comput Assist Tomogr       Date:  1987 Jul-Aug       Impact factor: 1.826

3.  New aspects of colobomas and optic nerve anomalies.

Authors:  D J Apple
Journal:  Int Ophthalmol Clin       Date:  1984

4.  Computed tomographic analysis of deformity and dimensional changes in the eyeball.

Authors:  D R Osborne; G N Foulks
Journal:  Radiology       Date:  1984-12       Impact factor: 11.105

Review 5.  Ocular involvement in the fetal alcohol syndrome.

Authors:  K Strömland
Journal:  Surv Ophthalmol       Date:  1987 Jan-Feb       Impact factor: 6.048

6.  [Vater or Vacterl syndrome (author's transl)].

Authors:  W Baumann; I Greinacher; P Emmrich; J Spranger
Journal:  Klin Padiatr       Date:  1976-07       Impact factor: 1.349

7.  The Meckel syndrome: clinicopathological findings in 67 patients.

Authors:  R Salonen
Journal:  Am J Med Genet       Date:  1984-08

8.  Colobomatous macrophthalmia with microcornea.

Authors:  J B Bateman; I H Maumenee
Journal:  Ophthalmic Paediatr Genet       Date:  1984-08

9.  Corneal involvement in autosomal dominant coloboma/microphthalmos.

Authors:  W G Pearce
Journal:  Can J Ophthalmol       Date:  1986-12       Impact factor: 1.882

10.  Microphthalmos with cyst: clinical presentations and computed tomographic findings.

Authors:  A Weiss; C Martinez; M Greenwald
Journal:  J Pediatr Ophthalmol Strabismus       Date:  1985 Jan-Feb       Impact factor: 1.402

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  33 in total

1.  Causes of blindness at the "Wiyata Guna" School for the Blind, Indonesia.

Authors:  R Sitorus; M Preising; B Lorenz
Journal:  Br J Ophthalmol       Date:  2003-09       Impact factor: 4.638

2.  Ophthalmologic findings in Aicardi syndrome.

Authors:  Gary Fruhman; Tanya N Eble; Nikki Gambhir; V Reid Sutton; Ignatia B Van den Veyver; Richard A Lewis
Journal:  J AAPOS       Date:  2012-06       Impact factor: 1.220

3.  The nanophthalmic macula.

Authors:  J C Serrano; P R Hodgkins; D S Taylor; G A Gole; A Kriss
Journal:  Br J Ophthalmol       Date:  1998-03       Impact factor: 4.638

Review 4.  Eye pathologies in neonates.

Authors:  Nyaish Mansoor; Tihami Mansoor; Mansoor Ahmed
Journal:  Int J Ophthalmol       Date:  2016-12-18       Impact factor: 1.779

5.  Unilateral Autosomal Recessive Anophthalmia in a Patient with Cystic Craniopharyngioma.

Authors:  Amandeep Kumar; Ankit Bansal; Ajay Garg; Bhawani S Sharma
Journal:  Neuroophthalmology       Date:  2014-04-25

Review 6.  The genetic contribution to the phenotype.

Authors:  U Wolf
Journal:  Hum Genet       Date:  1995-02       Impact factor: 4.132

7.  Late Presentation of Retinoblastoma in a Teen with Aicardi Syndrome.

Authors:  Patricia Y Akinfenwa; Patricia Chévez-Barrios; Clio A Harper; Dan S Gombos
Journal:  Ocul Oncol Pathol       Date:  2016-02-02

8.  Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14.

Authors:  Hui Li; Jia-Xin Wang; Cheng-Ye Wang; Ping Yu; Qiang Zhou; Yong-Gang Chen; Lu-Hang Zhao; Ya-Ping Zhang
Journal:  Hum Genet       Date:  2007-10-09       Impact factor: 4.132

9.  A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphyloma.

Authors:  M A Reddy; P J Francis; V Berry; K Bradshaw; R J Patel; E R Maher; R Kumar; S S Bhattacharya; A T Moore
Journal:  Br J Ophthalmol       Date:  2003-02       Impact factor: 4.638

10.  Clinical and genetic features of a dominantly-inherited microphthalmia pedigree from China.

Authors:  Changhong Yu; Zhengmao Hu; Jingzhi Li; Ting Liu; Kun Xia; Lixin Xie
Journal:  Mol Vis       Date:  2009-05-08       Impact factor: 2.367

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