Familial congenital nasolacrimal duct obstruction

Orpha code: 451612OMIM code: 149700

Definicja

A rare, genetic, otorhinolaryngological malformation characterized by congenital impatency of the nasolacrimal draingage system in various members of a family. Presentation is not specific and may include a uni- or bilateral medial canthal mass, dacryocystitis, nasal obstruction, periorbital cellulitis, and epiphora. Dacryocystocele and lacrimal puncta agenesis may be associated.

Disease data
Klasyfikacja

Morphological anomaly

Kod ORPHA
451612
Kod OMIM
149700
Kod ICD10
Q10.5
Kod ICD11
LA14.14

No additional description.

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