Literature DB >> 33614726

Hypotrichosis with Juvenile Macular Dystrophy in Saudi Arabia: A Case Report.

Azhar Ahmed1, Azhar Alali1, Osama Alsharif1,2, Adnan Kaki1.   

Abstract

Hypotrichosis with juvenile macular dystrophy is an autosomal recessive disorder due to a mutation in the CDH3 gene. As its name indicates, the disease classically presented with hypotrichosis and early visual impairment. We describe herein a family member with alopecia since birth associated with severe visual impairment in their early life. We suspect the diagnosis of hypotrichosis with juvenile macular dystrophy. Genetic testing confirms the clinical suspension. We emphasize the importance of genetic testing for proper genetic counseling.
Copyright © 2020 by S. Karger AG, Basel.

Entities:  

Keywords:  Blindness; Childhood alopecia; Genetic hair disorders; Hypotrichosis; Visual impairment

Year:  2020        PMID: 33614726      PMCID: PMC7879292          DOI: 10.1159/000511741

Source DB:  PubMed          Journal:  Skin Appendage Disord        ISSN: 2296-9160


  10 in total

1.  Hypotrichosis with cone-rod dystrophy in a patient with cadherin 3 (CDH3) mutation.

Authors:  F Nasser; L Mulahasanovic; M Alkhateeb; S Biskup; K Stingl; E Zrenner
Journal:  Doc Ophthalmol       Date:  2019-02-01       Impact factor: 2.379

2.  Characterizing Disease Burden and Progression of Geographic Atrophy Secondary to Age-Related Macular Degeneration.

Authors:  Usha Chakravarthy; Clare C Bailey; Robert L Johnston; Martin McKibbin; Rehna S Khan; Sajjad Mahmood; Louise Downey; Narendra Dhingra; Christopher Brand; Christopher J Brittain; Jeffrey R Willis; Sarah Rabhi; Anushini Muthutantri; Ronald A Cantrell
Journal:  Ophthalmology       Date:  2018-02-01       Impact factor: 12.079

3.  Hypotrichosis with juvenile macular dystrophy: a case report with molecular study.

Authors:  Lucas Perez Vicente; Simone Finzi; Remo Susanna; Terri L Young
Journal:  Arq Bras Oftalmol       Date:  2017 Jan-Feb       Impact factor: 0.872

4.  A missense mutation in CDH3, encoding P-cadherin, causes hypotrichosis with juvenile macular dystrophy.

Authors:  Margarita Indelman; Reuven Bergman; Raziel Lurie; Gabriele Richard; Benjamin Miller; Danny Petronius; Dan Ciubutaro; Rina Leibu; Eli Sprecher
Journal:  J Invest Dermatol       Date:  2002-11       Impact factor: 8.551

5.  Phenotypic diversity and mutation spectrum in hypotrichosis with juvenile macular dystrophy.

Authors:  Margarita Indelman; Christian P Hamel; Reuven Bergman; Ken K Nischal; Dorothy Thompson; Marie-Odile Surget; Michal Ramon; Hatam Ganthos; Benjamin Miller; Gabriele Richard; Raziel Lurie; Rina Leibu; Isabelle Russell-Eggitt; Eli Sprecher
Journal:  J Invest Dermatol       Date:  2003-11       Impact factor: 8.551

6.  Histopathology of hypotrichosis with juvenile macular dystrophy.

Authors:  Reuven Bergman; Marcela Sapir; Eli Sprecher
Journal:  Am J Dermatopathol       Date:  2004-06       Impact factor: 1.533

7.  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

8.  Hypotrichosis and juvenile macular dystrophy caused by CDH3 mutation: A candidate disease for retinal gene therapy.

Authors:  Mandeep S Singh; Suzanne Broadgate; Ranjana Mathur; Richard Holt; Stephanie Halford; Robert E MacLaren
Journal:  Sci Rep       Date:  2016-05-09       Impact factor: 4.379

9.  New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report.

Authors:  Fiona Blanco-Kelly; Luciana Rodrigues-Jacy da Silva; Iker Sanchez-Navarro; Rosa Riveiro-Alvarez; Miguel Angel Lopez-Martinez; Marta Corton; Carmen Ayuso
Journal:  BMC Med Genet       Date:  2017-01-07       Impact factor: 2.103

10.  Hypotrichosis with Juvenile Macular Dystrophy.

Authors:  Filipa Tavares Almeida; Rui Carneiro-Freitas; Regina Caldas; Ana Paula Vieira
Journal:  Int J Trichology       Date:  2018 Sep-Oct
  10 in total
  2 in total

1.  A Novel Pathogenic CDH3 Variant underlying Heredity Hypotrichosis Simplex detected by Whole-Exome Sequencing (WES)-A Case Report.

Authors:  Ayat Kadhi; Lamiaa Hamie; Christel Tamer; Georges Nemer; Mazen Kurban
Journal:  Cold Spring Harb Mol Case Stud       Date:  2022-08-05

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

Authors:  Giovanna Carnovale Scalzo; Adriano Carnevali; Gabriele Piccoli; Domenico Ceravolo; Donatella Bruzzichessi; Rodolfo Iuliano; Rossana Tallerico; Valentina Gatti; Giuseppe Giannaccare; Vincenzo Scorcia
Journal:  BMC Ophthalmol       Date:  2021-07-23       Impact factor: 2.209

  2 in total

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