Literature DB >> 34301208

Multimodal imaging of Hypotrichosis with juvenile macular dystrophy: a case report.

Giovanna Carnovale Scalzo1, Adriano Carnevali2, Gabriele Piccoli1, Domenico Ceravolo1, Donatella Bruzzichessi1, Rodolfo Iuliano3, Rossana Tallerico3, Valentina Gatti1, Giuseppe Giannaccare1, Vincenzo Scorcia1.   

Abstract

BACKGROUND: To report the first Italian case of hypotrichosis with juvenile macular dystrophy complicated by macular neovascularization diagnosed through multimodal imaging. CASE
PRESENTATION: An 11-year-old boy was referred to our Institution for bilateral maculopathy of unknown origin. Multimodal imaging helps the diagnosis of Juvenile Macular Dystrophy with Hypotrichosis (HJMD). Fundus examination showed several alterations of the retinal pigment epithelium and circular pigmented area of chorioretinal atrophy. Structural spectral domain optical coherence tomography (OCT) showed some backscattering phenomenon with several alterations of retinal pigment epithelium and photoreceptor layer in both eyes. Moreover, OCT showed hyperreflective lesion beneath the neuroepithelium in left eye. OCT angiography (OCT-A) revealed a pathologic neovascular network in choriocapillaris plexus, probably the result of a fibrovascular membrane. Multifocal electroretinograms (MfERGs) showed functional alterations in 12.22° of the central retina. In order to confirm the suspicion of HJMD, the child and both parents underwent genetic testing. Both parents resulted to be heterozygous healthy carriers of a single variation.
CONCLUSION: Multimodal imaging, in particular OCT-A, is a useful aid, along to clinical findings and genetics, for the diagnosis of inherited retinal dystrophies.
© 2021. The Author(s).

Entities:  

Keywords:  CH3 mutation; Case report; Juvenile macular dystrophy; MfERG; Optical coherence tomography angiography

Year:  2021        PMID: 34301208     DOI: 10.1186/s12886-021-02037-8

Source DB:  PubMed          Journal:  BMC Ophthalmol        ISSN: 1471-2415            Impact factor:   2.209


  20 in total

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Authors:  J M Burke; F Cao; P E Irving; C M Skumatz
Journal:  Invest Ophthalmol Vis Sci       Date:  1999-11       Impact factor: 4.799

2.  Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin.

Authors:  E Sprecher; R Bergman; G Richard; R Lurie; S Shalev; D Petronius; A Shalata; Y Anbinder; R Leibu; I Perlman; N Cohen; R Szargel
Journal:  Nat Genet       Date:  2001-10       Impact factor: 38.330

3.  Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings.

Authors:  M Indelman; R Leibu; A Jammal; R Bergman; E Sprecher
Journal:  Br J Dermatol       Date:  2005-09       Impact factor: 9.302

4.  Hypotrichosis with juvenile macular dystrophy: clinical and electrophysiological assessment of visual function.

Authors:  Rina Leibu; Anna Jermans; Ghantus Hatim; Benjamin Miller; Eli Sprecher; Ido Perlman
Journal:  Ophthalmology       Date:  2006-05       Impact factor: 12.079

5.  P-cadherin is a p63 target gene with a crucial role in the developing human limb bud and hair follicle.

Authors:  Yutaka Shimomura; Muhammad Wajid; Lawrence Shapiro; Angela M Christiano
Journal:  Development       Date:  2008-01-16       Impact factor: 6.868

6.  Phenotypic observations in "hypotrichosis with juvenile macular dystrophy" (recessive CDH3 mutations).

Authors:  Arif O Khan; Hanno J Bolz
Journal:  Ophthalmic Genet       Date:  2016-02-17       Impact factor: 1.803

7.  Molecular cloning of a human Ca2+-dependent cell-cell adhesion molecule homologous to mouse placental cadherin: its low expression in human placental tissues.

Authors:  Y Shimoyama; T Yoshida; M Terada; Y Shimosato; O Abe; S Hirohashi
Journal:  J Cell Biol       Date:  1989-10       Impact factor: 10.539

8.  Novel CDH3 mutations in hypotrichosis with juvenile macular dystrophy.

Authors:  M Indelman; J Eason; M Hummel; O Loza; M Suri; M J Leys; M Bayne; F L Schwartz; E Sprecher
Journal:  Clin Exp Dermatol       Date:  2007-03       Impact factor: 3.470

9.  CDH3 gene related hypotrichosis and juvenile macular dystrophy - A case with a novel mutation.

Authors:  Omer Karti; Saygin Abali; Ziya Ayhan; Eylem Gokmeydan; Serhad Nalcaci; Aylin Yaman; Ali Osman Saatci
Journal:  Am J Ophthalmol Case Rep       Date:  2017-06-26

10.  Analysis of protein-coding genetic variation in 60,706 humans.

Authors:  Monkol Lek; Konrad J Karczewski; Eric V Minikel; Kaitlin E Samocha; Eric Banks; Timothy Fennell; Anne H O'Donnell-Luria; James S Ware; Andrew J Hill; Beryl B Cummings; Taru Tukiainen; Daniel P Birnbaum; Jack A Kosmicki; Laramie E Duncan; Karol Estrada; Fengmei Zhao; James Zou; Emma Pierce-Hoffman; Joanne Berghout; David N Cooper; Nicole Deflaux; Mark DePristo; Ron Do; Jason Flannick; Menachem Fromer; Laura Gauthier; Jackie Goldstein; Namrata Gupta; Daniel Howrigan; Adam Kiezun; Mitja I Kurki; Ami Levy Moonshine; Pradeep Natarajan; Lorena Orozco; Gina M Peloso; Ryan Poplin; Manuel A Rivas; Valentin Ruano-Rubio; Samuel A Rose; Douglas M Ruderfer; Khalid Shakir; Peter D Stenson; Christine Stevens; Brett P Thomas; Grace Tiao; Maria T Tusie-Luna; Ben Weisburd; Hong-Hee Won; Dongmei Yu; David M Altshuler; Diego Ardissino; Michael Boehnke; John Danesh; Stacey Donnelly; Roberto Elosua; Jose C Florez; Stacey B Gabriel; Gad Getz; Stephen J Glatt; Christina M Hultman; Sekar Kathiresan; Markku Laakso; Steven McCarroll; Mark I McCarthy; Dermot McGovern; Ruth McPherson; Benjamin M Neale; Aarno Palotie; Shaun M Purcell; Danish Saleheen; Jeremiah M Scharf; Pamela Sklar; Patrick F Sullivan; Jaakko Tuomilehto; Ming T Tsuang; Hugh C Watkins; James G Wilson; Mark J Daly; Daniel G MacArthur
Journal:  Nature       Date:  2016-08-18       Impact factor: 49.962

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