Literature DB >> 23709337

Congenital glaucoma as an ophthalmic manifestation of Frank-Ter Haar syndrome.

Zeynep Aktas1, Emine Esra Karaca, Nurcan Dogan, Tugba Çakmak, Metin Unlu, Levent Tok, Murat Hasanreisoglu.   

Abstract

We report on a patient with Frank-Ter Haar syndrome that is associated with high intraocular pressures. A 21-day-old male patient was referred to our clinic for surgical treatment of congenital glaucoma. On ophthalmic examination, he had buphthalmos, mild corneal edema and high IOP readings in both eyes. The patient underwent uneventful trabeculotomy surgery, bilaterally. Marked bilateral anterior iris insertion was noted during the surgery. Childhood glaucoma may be associated with Frank-Ter Haar syndrome.

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Year:  2013        PMID: 23709337     DOI: 10.1007/s10792-013-9796-5

Source DB:  PubMed          Journal:  Int Ophthalmol        ISSN: 0165-5701            Impact factor:   2.031


  10 in total

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Journal:  Clin Dysmorphol       Date:  2003-07       Impact factor: 0.816

Review 2.  Frank-Ter Haar syndrome in a newborn.

Authors:  P Femitha; Rojo Joy; Bahubali D Gane; B Adhisivam; B Vishnu Bhat
Journal:  Indian J Pediatr       Date:  2011-10-29       Impact factor: 1.967

3.  Childhood glaucoma as an ophthalmic manifestation of Seckel syndrome.

Authors:  Zeynep Aktas; Nilay Yuksel; Serdar Kula; Ahmet Akman; Berati Hasanreisoglu
Journal:  J Glaucoma       Date:  2013 Apr-May       Impact factor: 2.503

Review 4.  Further delineation of Frank-ter Haar syndrome.

Authors:  Saskia M Maas; Hulya Kayserili; Jan Lam; Memnune Y Apak; Raoul C M Hennekam
Journal:  Am J Med Genet A       Date:  2004-12-01       Impact factor: 2.802

5.  Megalocornea associated with multiple skeletal anomalies: a new genetic syndrome?

Authors:  Y Frank; M Ziprkowski; A Romano; R Stein; M B Katznelson; B Cohen; R M Goodman
Journal:  J Genet Hum       Date:  1973-06

6.  X-linked or autosomal dominant, lethal in the male, inheritance of the Melnick-Needles (osteodysplasty) syndrome? A reappraisal.

Authors:  R J Gorlin; J Knier
Journal:  Am J Med Genet       Date:  1982-12

7.  Melnick-Needles syndrome: indication for an autosomal recessive form.

Authors:  B ter Haar; B Hamel; J Hendriks; J de Jager
Journal:  Am J Med Genet       Date:  1982-12

8.  Congenital glaucoma in a child with partial 1q duplication and 9p deletion.

Authors:  F D Verbraak; K Pogány; J W Pilon; C M Mooy; H F de France; R C Hennekam; E M Bleeker-Wagemakers
Journal:  Ophthalmic Paediatr Genet       Date:  1992-09

Review 9.  Autosomal recessive Melnick-Needles syndrome or ter Haar syndrome? Report of a patient and reappraisal of an earlier report.

Authors:  B C Hamel; J M Draaisma; A J Pinckers; C Boetes; R L Hoppe; H H Ropers; H G Brunner
Journal:  Am J Med Genet       Date:  1995-04-10

10.  Frank-ter Haar syndrome with unusual clinical features.

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Journal:  Eur J Med Genet       Date:  2009-03-19       Impact factor: 2.708

  10 in total
  2 in total

1.  The In Vivo Effects of the CB1-Positive Allosteric Modulator GAT229 on Intraocular Pressure in Ocular Normotensive and Hypertensive Mice.

Authors:  Elizabeth A Cairns; Anna-Maria Szczesniak; Alex J Straiker; Pushkar M Kulkarni; Roger G Pertwee; Ganesh A Thakur; William H Baldridge; Melanie E M Kelly
Journal:  J Ocul Pharmacol Ther       Date:  2017-07-18       Impact factor: 2.671

2.  Frank-ter Haar syndrome--additional findings?

Authors:  Taha Emre Köse; Cemil İşler; Ş Neslihan Şenel; Tolga Şitilci; İlknur Özcan; Nihan Aksakallı
Journal:  Dentomaxillofac Radiol       Date:  2016       Impact factor: 2.419

  2 in total

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