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Arrhinia

Known as: Underdevelopment of nose, Aplasia of the nose, Failure of development of nose 
Complete absence of all nasal structures. [HPO:probinson]
National Institutes of Health

Related topics

Related topics

7 relations

Broader (3)

Congenital AbnormalityCongenital absenceNose
Congenital hypoplasia of noseCyclocephalyFaceHOLOPROSENCEPHALY 2 (disorder)

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
MRI‐based Morphometric Analysis of Posterior Cranial Fossa in the Diagnosis of Chiari Malformation Type I
The diagnosis of Chiari malformation type I (CMI) relies on MRI identification of a tonsillar descent (TD) through the foramen… 
2014
2014
Assessment of the Impact of Oil and Gas Resource Exploration on the Environment of Selected Communities in Delta State, Nigeria
This paper assessed the "Impact of Oil and Gas Resource Exploration on the Environment" of Delta State oil producing communities… 
Review
2007
Review
2007
Second‐Trimester Prenatal Diagnosis of Total Arhinia
Arhinia is defined as the congenital absence of the nose. It is an extremely rare condition, which is usually associated with… 
Review
2007
Review
2007
Prevalência de agenesia em uma clínica ortodôntica de Goiânia
Objetivos : Estudar a prevalencia de agenesia em uma clinica de ortodontia na cidade de Goiânia, atraves do exame radiografico… 
2005
2005
1 Improving Teaching and Learning through Effective Incentives Lessons from Education Reforms in Latin America
As a region, Latin America faces tremendous challenges, particularly those of development, poverty, and inequality. Education is… 
Review
2003
Review
2003
Prenatal sonographic features of Harlequin ichthyosis
Abstract. Harlequin ichthyosis (HI) is a severe and usually fatal congenital keratinization disorder with autosomal recessive… 
2003
2003
An unusual case of heminasal aplasia: proboscis lateralis or cystic teratoma?
Unilateral aplasia of the nose is a rare congenital malformation. It is often associated with other malformations of the facial… 
Review
2001
Review
2001
Congenital absence of the nose: a case report and literature review
Abstract A case of congenital absence of the nose is presented. The etiology of this rare condition is unknown. A review of the… 
Review
1997
Review
1997
Heminasal aplasia: a case report and review of the literature of the last 25 years
We report a child with right-sided heminasal aplasia in combination with anomalies of the right eye and maxilia Unilateral… 
1993
1993
Steinfeld syndrome: report of a second family and further delineation of a rare autosomal dominant disorder.
We report on a fetus with alobar holoprosencephaly, microphthalmia, midline cleft lip and palate, absent nose, dysplastic ears… 
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