Term newborn with microphthalmia, encephalocele and linear skin defect
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DOI:
https://doi.org/10.26326/2281-9649.31.2.2236How to Cite
Franco Fuenmayor M.E., Huff M.L. 2021. Term newborn with microphthalmia, encephalocele and linear skin defect. Eur. J. Pediat. Dermatol. 31 (2):95-98. 10.26326/2281-9649.31.2.2236.
pp. 95-98
Abstract
The presence of skin and ocular findings includes syndromes with X linked transmission, such as microphthalmia with linear skin defects (MLS) syndrome, focal dermal hypoplasia (Goltz syndrome), oculocerebrocutaneous syndrome, incontinentia pigmenti and Aicardi syndrome. We report the case of a term neonate with corneal opacities and unusual skin findings along with an encephalocele consistent with MLS syndrome.
Keywords
corneal opacity, encephalocele, skin