Term newborn with microphthalmia, encephalocele and linear skin defect

DOI:

https://doi.org/10.26326/2281-9649.31.2.2236

How 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.

Authors

Franco Fuenmayor M.E. Huff M.L.
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