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Petraevskiĭ A.V.

GBOU VPO "Volgogradskiĭ gosudarstvennyĭ meditsinskiĭ universitet" Minzdravsotsrazvitiia Rossii

Familial case of Axenfeld anomaly associated with Shtargardt dystrophy

Authors:

Petraevskiĭ A.V.

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Journal: Russian Annals of Ophthalmology. 2012;128(5): 39‑43

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To cite this article:

Petraevskiĭ AV. Familial case of Axenfeld anomaly associated with Shtargardt dystrophy. Russian Annals of Ophthalmology. 2012;128(5):39‑43. (In Russ.)

Подписка 2025 (Russian Annals of Ophthalmology)
 
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A clinical case of Axenfeld anomaly (posterior embryotoxon) in a 3-generation family is presented. However mother and father are not related to each other. A son who had the most prominent clinical manifestation had a typical bilateral Shtargardt dystrophy.

Keywords:

posterior embryotoxon
Axenfeld anomaly
Shtargardt dystrophy

Authors:

Petraevskiĭ A.V.

GBOU VPO "Volgogradskiĭ gosudarstvennyĭ meditsinskiĭ universitet" Minzdravsotsrazvitiia Rossii

List of references:

  1. Vodovozov A.M. Svetovye refleksy glaznogo dna. M 1980.
  2. Kanski D.D. Klinicheskaya oftal'mologiya: sistematizirovannyi podkhod. M 2006.
  3. Koskas G., Koskas F., Zurdan A. Kompleksnaya diagnostika patologii glaznogo dna. M 2007.
  4. Krachmer D., Pelei D. Rogovitsa. Atlas. M 2007.
  5. Petraevskii A.V., Gndoyan I.A., Balalin S.V. Semeino-nasledstvennyi sluchai sindroma Rigera s vtorichnoi glaukomoi (klinicheskoe nablyudenie). Glaukoma 2006; 4: 45-50.
  6. Teilor D., Khoit K. Detskaya oftal'mologiya. M 2007.
  7. Spallone A. Retinal detachment in Axenfeld - Rieger syndrome. Brit J Ophthalmol 1989; .73: 559-562.

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