Literature DB >> 739340

Congenital Leber amaurosis, keratoconus, and mental retardation in familial juvenile nephronophtisis.

V Godel, M Blumenthal, A Iaina.   

Abstract

Two siblings suffering from congenital Leber amaurosis were found to be affected also by juvenile nephronophtisis. Keratoconus in one child and mental retardation in the other developed during their later growth. An extensive laboratory study showed normal results but revealed an impaired urinary concentrating ability. The hereditary pattern operating in this complex disease was found to be consistent with an autosomal recessive trait.

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Mesh:

Year:  1978        PMID: 739340     DOI: 10.3928/0191-3913-19780301-09

Source DB:  PubMed          Journal:  J Pediatr Ophthalmol Strabismus        ISSN: 0191-3913            Impact factor:   1.402


  5 in total

1.  Sector retinitis pigmentosa in juvenile nephronophthisis.

Authors:  V Godel; A Iaina; P Nemet; M Lazar
Journal:  Br J Ophthalmol       Date:  1980-02       Impact factor: 4.638

2.  Hereditary renal-retinal dysplasia.

Authors:  V Godel; A Iaina; P Nemet; M Lazar
Journal:  Doc Ophthalmol       Date:  1980-10-15       Impact factor: 2.379

3.  Transepithelial versus epithelium-off corneal crosslinking for progressive keratoconus.

Authors:  Sueko M Ng; Mark Ren; Kristina B Lindsley; Barbara S Hawkins; Irene C Kuo
Journal:  Cochrane Database Syst Rev       Date:  2021-03-23

Review 4.  Corneal cross-linking treatment of keratoconus.

Authors:  Mahgol Farjadnia; Mohammad Naderan
Journal:  Oman J Ophthalmol       Date:  2015 May-Aug

Review 5.  Gene therapy in keratoconus.

Authors:  Mahgol Farjadnia; Mohammad Naderan; Mehrdad Mohammadpour
Journal:  Oman J Ophthalmol       Date:  2015 Jan-Apr
  5 in total

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