Literature DB >> 24547910

Ophthalmologic Findings in H Syndrome: A Unique Diagnostic Clue.

Vered Molho-Pessach1,2, Hadas Mechoulam3, Rula Siam1, Sofia Babay2, Yuval Ramot1,2, Abraham Zlotogorski1,2.   

Abstract

BACKGROUND: H syndrome is an autosomal recessive histiocytosis with multisystemic involvement caused by mutations in the SLC29A3 gene. The term H syndrome was coined to denote the major clinical findings which include hyperpigmentation, hypertrichosis, hearing loss, hepatosplenomegaly, hypogonadism, hyperglycemia/diabetes mellitus and hallux valgus/flexion contractures. Almost 100 individuals affected with this disorder have been reported, however, a thorough evaluation of the ophthalmologic features of H syndrome has not yet been performed.
MATERIALS AND METHODS: Ophthalmic examination of a 50-year-old male with H syndrome. Mutation analysis of SLC29A3 was also performed in this patient.
RESULTS: Ophthalmic findings included; shallow orbits with exorbitism, bilateral pterygium, limbal thickening, corneal arcus and cortical cataract. We also review ophthalmologic findings in previously reported H syndrome patients.
CONCLUSIONS: The presence of dilated lateral scleral vessels, corneal arcus and shallow orbits should raise the suspicion of H syndrome, especially when seen in young age.

Entities:  

Keywords:  Corneal arcus; H syndrome; SLC29A3; histiocytosis

Mesh:

Substances:

Year:  2014        PMID: 24547910     DOI: 10.3109/13816810.2014.886272

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


  5 in total

1.  Identification of a novel mutation in solute carrier family 29, member 3 in a Chinese patient with H syndrome.

Authors:  Jia-Wei Liu; Nuo Si; Lian-Qing Wang; Ti Shen; Xue-Jun Zeng; Xue Zhang; Dong-Lai Ma
Journal:  Chin Med J (Engl)       Date:  2015-05-20       Impact factor: 2.628

2.  The histopathology and phenotypic variability in H syndrome.

Authors:  David Dias-Polak; Margarita Indelman; Reuven Bergman; Emily Avitan-Hersh
Journal:  Clin Case Rep       Date:  2018-01-25

3.  H Syndrome: A Case Report and Review of Literature.

Authors:  Dilip Meena; Payal Chauhan; Neirita Hazarika; Naveen Kumar Kansal
Journal:  Indian J Dermatol       Date:  2018 Jan-Feb       Impact factor: 1.494

4.  Bilateral Double-headed Recurrent Pterygium: A Case Presentation and Literature Review.

Authors:  Bengi Ece Kurtul; Ahmet Kakac; Abdulkerim Karaaslan
Journal:  Med Hypothesis Discov Innov Ophthalmol       Date:  2020-03-15

5.  Phenotypic intrafamilial variability including H syndrome and Rosai-Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 gene.

Authors:  Hamza Chouk; Mohamed Ben Rejeb; Lobna Boussofara; Haїfa Elmabrouk; Najet Ghariani; Badreddine Sriha; Ali Saad; Dorra H'Mida; Mohamed Denguezli
Journal:  Hum Genomics       Date:  2021-10-17       Impact factor: 4.639

  5 in total

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