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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.
2016
2016
Bosma arrhinia microphthalmia syndrome in a Mexican patient with a molecular analysis of PAX6
The association of anophthalmia, arrhinia, and hypogonadism constitutes the major clinical features for Bosma arrhinia… 
2013
2013
Hypogonadotropic hypogonadism presenting with arhinia: a case report
IntroductionArhinia, congenital absence of the nose, is a rare malformation. We present the third reported case of arhinia… 
2011
2011
Developing Rwanda's schools infrastructure standards and guidelines
Purpose – The purpose of this paper is to share the experience of those directly involved in drafting the new national school… 
2009
2009
Agenesia del Tercer Molar en una Etnia Originaria del Norte de Chile: Aymaras
Agenesia es la ausencia de dientes por alteraciones geneticas aisladas o sindromicas. La agenesia del tercer molar esta asociada… 
2007
2007
Síndrome de Rokitansky (agenesia úterovaginal): aspectos clínicos, diagnósticos y terapéuticos
Correspondencia: Dra. María E. Escobar meugeniaescobar@ yahoo.com.ar RESUMEN Introducción. El síndrome de Rokitansky es una… 
2007
2007
Universities, innovation and development processes in the changing global economy
Universities are undergoing a process of remaking all over the world, including developing countries. The importance of… 
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… 
1994
1994
[Considerations concerning respiratory physiopathology in a case of total arhinia].
The Authors describe their personal experience in a rare case of total arhinia in a young boy, now seven years old, whose psycho… 
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… 
1975
1975
Overcoming Underdevelopment. A Research Paradigm
1. On the Genesis of Underdevelopment The evolution of the capitalist mode of production on a world scale entailed an unequal… 
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