نتایج جستجو برای: congenital distichiasis
تعداد نتایج: 120364 فیلتر نتایج به سال:
Purpose: To evaluate the use of amniotic membrane transplantation (AMT) for management of congenital distichiasis. Methods: In this interventional case series, 16 eyelids of 5 patients with congenital distichiasis underwent posterior lamella resection and AMT. Results: All patients were male subjects with mean age of 13.6±15.2 (range 2-42) years. Mean follow up was 17±7.5 (range 6-29) months. D...
purpose: to evaluate the use of amniotic membrane transplantation (amt) for management of congenital distichiasis. methods: this interventional case series was performed on 16 eyelids of 5 patients with congenital distichiasis treated with posterior lamella resection and amt. results: all patients were men aged 2 to 42 years. mean follow up was 17 months (6-29 months). post-operative symptoms o...
Distichiasis is the congenital condition of partial or complete accessory rows of eyelashes which exit from the posterior lid margin at or near the meibomian gland orifices. A series of 24 patients with distichiasis is presented with clinical features and results of treatment. The treatment modes of epilation, lid margin cryotherapy, or eyelid splitting cryotherapy to the posterior lamella are ...
INTRODUCTION Lymphoedema-distichiasis syndrome (LD) (OMIM 153400) is a rare, primary lymphoedema of pubertal onset, associated with distichiasis. Causative mutations have now been described in FOXC2, a forkhead transcription factor gene. Numerous clinical associations have been reported with this condition, including congenital heart disease, ptosis, varicose veins, cleft palate, and spinal ext...
Distichiasis presents as double rows of eyelashes arising from aberrant differentiation of the meibomian glands of the eyelids, and it may be sporadic or hereditary. FOXC2 gene mutations in hereditary distichiasis are rarely reported. Here, we examined two generations of a Chinese family with hereditary distichiasis but without lymphedema or other features of LD syndrome. The FOXC2 gene was amp...
BACKGROUND Hereditary lymphoedema-distichiasis (LD) is an autosomal dominant disorder that classically presents as lymphoedema of the limbs, with variable age of onset, and extra aberrant growth of eyelashes from the Meibomian gland (distichiasis). Other major reported complications include cardiac defects, cleft palate, and extradural cysts. Photophobia, exotropia, ptosis, congenital ectropion...
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