Congenital bilateral ectropion in lamellar ichthyosis
نویسندگان
چکیده
منابع مشابه
Ocular manifestations of congenital lamellar ichthyosis.
PURPOSE To describe the ophthalmic manifestations in a series of children with congenital lamellar ichthyosis. These cases presented with varying types of eyelid abnormality associated with the systemic disease. The clinical features and ophthalmic management were studied. METHODS The case histories of three children presenting to the oculoplastic clinic were reviewed. All were diagnosed with...
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Purpose: To report a case of bilateral congenital Ectropion and its management. Case Report: A newborn with bilateral congenital upper eyelid Ectropion and sign of exposure keratopathy associated with bilateral cleft lip and palate was referred and underwent full thickness skin graft of both upper eyelids. Ectropion was corrected and sign of exposure keratopathy improved. Conclusion: Congenital...
متن کاملLamellar ichthyosis presenting as bilateral spontaneous corneal perforation.
INTRODUCTION Lamellar Ichthyosis is an autosomal recessive, inherited skin disorder characterized by thickening, fissuring and scaling of the skin. OBJECTIVE To report a case of lamellar icthyosis and highlight the importance of monitoring corneal health in these patients. CASE We report a rare case of bilateral spontaneous corneal perforation in a patient with lamellar ichthyosis .The pati...
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Lamellar ichthyosis (LI) is a rare genetic disorder with autosomal recessive inheritance. It is equally seen in both sexes and usually manifests at birth. The child presents as a collodion baby. The erythema is minimal or absent; but when present, it is maximum on the face. The scaling is generalized, accentuated on lower extremities and flexural areas. Rickets is a condition in which there is ...
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Bilateral Congenital Eublepharon, also referred to as ectropion, is a rare condition in which at birth the eyelids do not cover the eye. It is more commonly found in Afro-Caribbean infants and in those with trisomy 21. Management is usually conservative. We review data from animal embryology to propose the condition may be related to defects in the expression of fibroblast growth factor 2 (FGFR...
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ژورنال
عنوان ژورنال: Oman Journal of Ophthalmology
سال: 2011
ISSN: 0974-620X
DOI: 10.4103/0974-620x.77662