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Case report

https://doi.org/10.13112/PC.2020.31

Congenital alacrima in a 17-month-old boy: a case report

Freja Bagatin
Renata Iveković
Adriana Bobinec
Maja Malenica Ravlić
Zoran Vatavuk


Full text: english pdf 648 Kb

page 200-206

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Full text: croatian pdf 648 Kb

page 200-206

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Abstract

Alacrima is a rare disorder defined as decreased or absent tear production that is mostly manifested from birth. It may occur as isolated due to congenital aplasia/hypoplasia or impaired innervation of the lacrimal gland and associated structures, but it may also
be part of a rare, predominantly genetic disorder. We present a case of a boy with congenital alacrima, discuss diagnostic work-up
and review differential diagnosis of dry eye with emphasis on disorders that occur in childhood.

Keywords

LACRIMAL APPARATUS DISEASES – congenital, genetics, diagnosis; DRY EYE SYNDROMES

Hrčak ID:

251902

URI

https://hrcak.srce.hr/251902

Publication date:

30.9.2020.

Article data in other languages: croatian

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