Literature DB >> 32195884

OCULAR MANIFESTATIONS OF PORETTI-BOLTSHAUSER SYNDROME: FINDINGS FROM MULTIMODAL IMAGING AND ELECTROPHYSIOLOGY.

Cindy X Cai1, Michelle Go1, Michael P Kelly1, Sandra Holgado1, Cynthia A Toth1,2.   

Abstract

BACKGROUND/
PURPOSE: Poretti-Boltshauser syndrome is a rare, nonprogressive neurologic syndrome with characteristic cerebellar cysts on neuroimaging due to mutations in LAMA1. The ophthalmic findings in Poretti-Boltshauser syndrome are not well described. Here, we report the ophthalmic findings from multimodal imaging and electrophysiology of a patient with genetically confirmed Poretti-Boltshauser syndrome.
METHODS: A 3-year-old boy with confirmed mutations in LAMA1 underwent examination under anesthesia with electroretinography and multimodal imaging including fundus photography, fluorescein angiography, optical coherence tomography, and optical coherence tomography angiography.
RESULTS: Dilated fundus examination was notable for retinal vascular anomalies, including a large area of nonperfusion in the temporal macula with corresponding retinal thinning on optical coherence tomography. There was an absence of a distinct foveal avascular zone and decreased density of both the superficial and deep vascular plexuses in the macula on optical coherence tomography angiography. There was diffuse loss of choriocapillaris architecture and decreased choroidal thickness.
CONCLUSION: Patients with Poretti-Boltshauser syndrome may possess chorioretinal thinning and retinal vascular abnormalities appreciable on examination and multimodal imaging. These findings suggest a role for LAMA1 in retinal and choroidal vascular development.

Entities:  

Mesh:

Year:  2020        PMID: 32195884      PMCID: PMC7494654          DOI: 10.1097/ICB.0000000000000991

Source DB:  PubMed          Journal:  Retin Cases Brief Rep        ISSN: 1935-1089


  10 in total

1.  Type IV collagen and laminin in Bruch's membrane and basal linear deposit in the human macula.

Authors:  G E Marshall; A G Konstas; G G Reid; J G Edwards; W R Lee
Journal:  Br J Ophthalmol       Date:  1992-10       Impact factor: 4.638

2.  Retinal Avascularity and Neovascularization Associated With LAMA1 (laminin1) Mutation in Poretti-Boltshauser Syndrome.

Authors:  Elizabeth Marlow; R V Paul Chan; Erica Oltra; Irene Rusu; Mrinali P Gupta
Journal:  JAMA Ophthalmol       Date:  2018-01-01       Impact factor: 7.389

Review 3.  The emerging role of tetraspanin microdomains on endothelial cells.

Authors:  Rebecca L Bailey; John M Herbert; Kabir Khan; Victoria L Heath; Roy Bicknell; Michael G Tomlinson
Journal:  Biochem Soc Trans       Date:  2011-12       Impact factor: 5.407

4.  Laminin-α1 LG4-5 domain binding to dystroglycan mediates muscle cell survival, growth, and the AP-1 and NF-κB transcription factors but also has adverse effects.

Authors:  Yan Wen Zhou; Jesus Munoz; Daifeng Jiang; Harry W Jarrett
Journal:  Am J Physiol Cell Physiol       Date:  2011-12-07       Impact factor: 4.249

5.  Ocular findings in a case of Pierson syndrome with a novel mutation in laminin ß2 gene.

Authors:  Mitsuru Arima; Shoko Tsukamoto; Rumi Akiyama; Kei Nishiyama; Ri-Ichiro Kohno; Takashi Tachibana; Akira Hayashida; Miwa Murayama; Toshio Hisatomi; Kandai Nozu; Kazumoto Iijima; Shouichi Ohga; Koh-Hei Sonoda
Journal:  J AAPOS       Date:  2018-08-16       Impact factor: 1.220

6.  Astrocytes follow ganglion cell axons to establish an angiogenic template during retinal development.

Authors:  Matthew L O'Sullivan; Vanessa M Puñal; Patrick C Kerstein; Joseph A Brzezinski; Tom Glaser; Kevin M Wright; Jeremy N Kay
Journal:  Glia       Date:  2017-07-19       Impact factor: 7.452

7.  Cystic cerebellar dysplasia and biallelic LAMA1 mutations: a lamininopathy associated with tics, obsessive compulsive traits and myopia due to cell adhesion and migration defects.

Authors:  Thierry Vilboux; May Christine V Malicdan; Yun Min Chang; Jennifer Guo; Patricia M Zerfas; Joshi Stephen; Andrew R Cullinane; Joy Bryant; Roxanne Fischer; Brian P Brooks; Wadih M Zein; Edythe A Wiggs; Christopher K Zalewski; Andrea Poretti; Melanie M Bryan; Meghana Vemulapalli; James C Mullikin; Martha Kirby; Stacie M Anderson; Marjan Huizing; Camilo Toro; William A Gahl; Meral Gunay-Aygun
Journal:  J Med Genet       Date:  2016-01-13       Impact factor: 6.318

8.  Mutations in LAMA1 cause cerebellar dysplasia and cysts with and without retinal dystrophy.

Authors:  Kimberly A Aldinger; Stephen J Mosca; Martine Tétreault; Jennifer C Dempsey; Gisele E Ishak; Taila Hartley; Ian G Phelps; Ryan E Lamont; Diana R O'Day; Donald Basel; Karen W Gripp; Laura Baker; Mark J Stephan; Francois P Bernier; Kym M Boycott; Jacek Majewski; Jillian S Parboosingh; A Micheil Innes; Dan Doherty
Journal:  Am J Hum Genet       Date:  2014-08-07       Impact factor: 11.025

9.  Mutations in Lama1 disrupt retinal vascular development and inner limiting membrane formation.

Authors:  Malia M Edwards; Elmina Mammadova-Bach; Fabien Alpy; Annick Klein; Wanda L Hicks; Michel Roux; Patricia Simon-Assmann; Richard S Smith; Gertraud Orend; Jiang Wu; Neal S Peachey; Jürgen K Naggert; Olivier Lefebvre; Patsy M Nishina
Journal:  J Biol Chem       Date:  2010-01-04       Impact factor: 5.157

10.  Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti-Boltshauser syndrome).

Authors:  Alessia Micalizzi; Andrea Poretti; Marta Romani; Monia Ginevrino; Tommaso Mazza; Chiara Aiello; Ginevra Zanni; Bastian Baumgartner; Renato Borgatti; Knut Brockmann; Ana Camacho; Gaetano Cantalupo; Martin Haeusler; Christiane Hikel; Andrea Klein; Giorgia Mandrile; Eugenio Mercuri; Dietz Rating; Romina Romaniello; Filippo Maria Santorelli; Mareike Schimmel; Luigina Spaccini; Serap Teber; Arpad von Moers; Sarah Wente; Andreas Ziegler; Andrea Zonta; Enrico Bertini; Eugen Boltshauser; Enza Maria Valente
Journal:  Eur J Hum Genet       Date:  2016-03-02       Impact factor: 4.246

  10 in total

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