Literature DB >> 19390472

Albinism: classification, clinical characteristics, and recent findings.

C Gail Summers1.   

Abstract

PURPOSE: To describe the clinical characteristics and recent findings in the heterogeneous group of inherited disorders of melanin biosynthesis grouped as "albinism."
METHODS: The current classification of albinism, and the cutaneous, ocular, and central nervous system characteristics are presented. Recent clinical findings are summarized.
RESULTS: Albinism is now classified based on genes known to be responsible for albinism. Foveal hypoplasia is invariably present and individuals with albinism often have delayed visual development, reduced vision, nystagmus, a positive angle kappa, strabismus, iris transillumination, and absent or reduced melanin pigment in the fundi. A visual-evoked potential can document the excessive retinostriate decussation seen in albinism. Grating acuity can be used to document delayed visual development in preverbal children. Glasses are often needed to improve visual acuity and binocular alignment.
CONCLUSIONS: Albinism is caused by several different genes. Heterogeneity in clinical phenotype indicates that expressivity is variable.

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Mesh:

Year:  2009        PMID: 19390472     DOI: 10.1097/OPX.0b013e3181a5254c

Source DB:  PubMed          Journal:  Optom Vis Sci        ISSN: 1040-5488            Impact factor:   1.973


  27 in total

Review 1.  What we know about the generation of nystagmus and other ocular oscillations: are we closer to identifying therapeutic targets?

Authors:  Rebecca Jane McLean; Irene Gottlob; Frank Antony Proudlock
Journal:  Curr Neurol Neurosci Rep       Date:  2012-06       Impact factor: 5.081

2.  [Hermansky-Pudlak syndrome].

Authors:  A Atili; J Lübke; M Shoukier; M P Schittkowski
Journal:  Ophthalmologe       Date:  2013-02       Impact factor: 1.059

3.  Keratinocyte-derived laminin-332 protein promotes melanin synthesis via regulation of tyrosine uptake.

Authors:  Heesung Chung; Hyejung Jung; Jung-Hyun Lee; Hye Yun Oh; Ok Bin Kim; Inn-Oc Han; Eok-Soo Oh
Journal:  J Biol Chem       Date:  2014-06-20       Impact factor: 5.157

4.  Arrested development: high-resolution imaging of foveal morphology in albinism.

Authors:  John T McAllister; Adam M Dubis; Diane M Tait; Shawn Ostler; Jungtae Rha; Kimberly E Stepien; C Gail Summers; Joseph Carroll
Journal:  Vision Res       Date:  2010-02-10       Impact factor: 1.886

5.  Quality of life in patients with oculocutaneous albinism.

Authors:  Marcus Maia; Beatrice Mussio Fornazier Volpini; Gabriela Alves dos Santos; Maria Josefa Penon Rujula
Journal:  An Bras Dermatol       Date:  2015 Jul-Aug       Impact factor: 1.896

6.  Ocular findings in patients with oculocutaneous albinism type ia with G47D tyrosinase gene mutation in Puerto Rico: a case report.

Authors:  Ferdinand Rodríguez-Agramonte; Natalio J Izquierdo; Carmen Cadilla
Journal:  Bol Asoc Med P R       Date:  2013

7.  Molecular analysis of Korean patients with oculocutaneous albinism.

Authors:  Shin Hae Park; Hyojin Chae; Yonggoo Kim; Myungshin Kim
Journal:  Jpn J Ophthalmol       Date:  2011-11-01       Impact factor: 2.447

8.  Prevalence and profile of ophthalmic disorders in oculocutaneous albinism: a field report from South-Eastern Nigeria.

Authors:  N N Udeh; B I Eze; S N Onwubiko; O C Arinze; E N Onwasigwe; R E Umeh
Journal:  J Community Health       Date:  2014-12

9.  Prosthodontic management of an albinism patient-dental implications and management.

Authors:  Varsha Murthy; Yuvraj V; Shaji Thomas; Preeti Nair
Journal:  BMJ Case Rep       Date:  2013-01-22

Review 10.  Pigmentation and vision: Is GPR143 in control?

Authors:  Brian S McKay
Journal:  J Neurosci Res       Date:  2018-05-14       Impact factor: 4.164

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