Complete nasal agenesis with bilateral microphthalmia and unilateral duplication of the thumb

Complete nasal aplasia is an extremely rare clinical entity and most infants are stillborn when this is associated with holoprosencephaly. A viable 3-year-old infant born with frontonasal arrest without holoprosencephaly is presented. The child's main complaint was lack of a nasal airway, which...

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Veröffentlicht in:Plastic and reconstructive surgery (1963) 1995-05, Vol.95 (6), p.1101-1104
Hauptverfasser: LATRENTA, G. S, CHOI, H. W, WARD, R. F, HOFFMAN, L, NEIDICH, J. A
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container_end_page 1104
container_issue 6
container_start_page 1101
container_title Plastic and reconstructive surgery (1963)
container_volume 95
creator LATRENTA, G. S
CHOI, H. W
WARD, R. F
HOFFMAN, L
NEIDICH, J. A
description Complete nasal aplasia is an extremely rare clinical entity and most infants are stillborn when this is associated with holoprosencephaly. A viable 3-year-old infant born with frontonasal arrest without holoprosencephaly is presented. The child's main complaint was lack of a nasal airway, which made eating extremely difficult. A method for craniofacial reconstruction of the nasopharynx is presented.
doi_str_mv 10.1097/00006534-199505000-00024
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ispartof Plastic and reconstructive surgery (1963), 1995-05, Vol.95 (6), p.1101-1104
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source MEDLINE; Journals@Ovid Complete
subjects Abnormalities, Multiple - surgery
Biological and medical sciences
Child, Preschool
Head and neck surgery. Maxillofacial surgery. Dental surgery. Orthodontics
Humans
Male
Medical sciences
Microphthalmos - surgery
Nasopharynx - surgery
Nose - abnormalities
Nose - surgery
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Surgery of the upper aerodigestive tract
Thumb - abnormalities
title Complete nasal agenesis with bilateral microphthalmia and unilateral duplication of the thumb
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