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Titlebook: Aniridia; Recent Developments Mohit Parekh,Barbara Poli,Diego Ponzin Book 2015 Springer International Publishing Switzerland 2015 Aniridia

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樓主: cerebral-cortex
51#
發(fā)表于 2025-3-30 08:31:21 | 只看該作者
Strategies for Success in Limbal Allograft Transplantation for Aniridia,arring occurred. More recently, keratolimbal allograft (KLAL) has been shown to be an effective treatment. In this chapter we discuss how to maximize the visual outcome of aniridic keratopathy patients. Glaucoma should be addressed by placing shunts in patients prior to KLAL in order to limit topica
52#
發(fā)表于 2025-3-30 15:50:28 | 只看該作者
The Paediatric Patient: Identifying Congenital Aniridia as Soon as Possible,essively impair vision in multiple causes including keratopathy, cataract, glaucoma, foveal hypoplasia, nystagmus. Aniridia is a genetic haplo-insufficiency expression of the PAX6 gene located on the chromosome 11p13. Aniridia, genital anomalies, retardation and Wilms tumor are called WAGR Syndrome.
53#
發(fā)表于 2025-3-30 20:01:28 | 只看該作者
Aniridia: Early Diagnosis: The Key Roles of Neonatologists, Paediatricians and Paediatric Ophthalmo worsened by the complications associated with the disease such as glaucoma, corneal clouding and cataract. The genetics include a mutation in the PAX6-gene on chromosome 11p13. More extensive alterations on the chromosome 11p may include the WT1-gene (Wilms tumor gene) which may cause WAGR-syndrome
54#
發(fā)表于 2025-3-30 23:57:38 | 只看該作者
,Aniridia Guides and Aniridia-Syndrome (PAX6-Syndrome): Do’s and Dont’s in Clinical Care,dromes including WAGR- and WAGRO-syndrome and other syndromes with intellectual impairment. Furthermore, recent research shows that aniridia associated with alterations in the PAX6 gene often shows further systemic implications (endocrine, metabolic and neurological pathologies). Therefore, PAX6-rel
55#
發(fā)表于 2025-3-31 02:36:39 | 只看該作者
56#
發(fā)表于 2025-3-31 07:53:28 | 只看該作者
57#
發(fā)表于 2025-3-31 12:41:12 | 只看該作者
58#
發(fā)表于 2025-3-31 13:49:43 | 只看該作者
,What to Do When Diagnosed with Aniridia: The Role of Patients’ Associations – Bringing Together Supsorder was not fully understood until recently. Today the disorder is known as “aniridia syndrome” since research has shown that the PAX6 gene is responsible for more than just development of the eyes. It has been found that the role of PAX6 can have systemic effects as well; although more research
59#
發(fā)表于 2025-3-31 20:56:49 | 只看該作者
60#
發(fā)表于 2025-3-31 22:36:33 | 只看該作者
ia affects between 1:40,000 to 1:100,000 people, and affects males and females equally. People with Aniridia may also experience secondary conditions such as Photophobia, Nystagmus, Glaucoma, Cataracts and Keratopathy. ?978-3-319-36394-3978-3-319-19779-1
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