Results 41 to 50 of about 55,513 (351)

Evaluation of the relationship between the presence of an accessory maxillary ostium and the presence and types of nasal septum deviation: A computed tomography study. [PDF]

North Clin Istanb
Duzkalir HG, Karaoysal OA, Rona G.
europepmc   +3 more sources

Comparison of pathological findings and accumulation of fluorin-18 fluorodeoxyglucose on positron emission tomography/computed tomography: A case of relapsing polychondritis

Respiratory Medicine Case Reports, 2023
A 70-year-old woman with a hoarse voice and dry cough was referred to our hospital. Positron emission tomography/computed tomography showed abnormal accumulation of fluorine-18 fluorodeoxyglucose (FDG) at the nasal septum, larynx, trachea, bronchus, and ...
Hirokazu Tokuyasu, Haruka Watanabe, Yuriko Sueda, Hiromitsu Sakai, Natsumi Omura-Tanaka, Kenichirou Nakajima, Satoru Nakamatsu, Chika Esumi, Akira Yamasaki   +8 more
doaj   +1 more source

Pitfalls in Cytodiagnosis of Pleomorphic Adenoma of the Nasal Septum - A Rare Case Report [PDF]

, 2010
Pleomorphic adenoma is the most common benign mixed tumor of major salivary gland. Ectopic occurrence of pleomorphic adenoma are seen in minor salivary glands of pharynx, trachea, larynx and very rarely in nasal septum.
Krishnappa, Amitha, MG, Abhishek, S, Vijayshankar   +2 more
core  

On the development of the chondrocranium and the histological anatomy of the head in perinatal stages of marsupial mammals [PDF]

, 2017
An overview of the literature on the chondrocranium of marsupial mammals reveals a relative conservatism in shape and structures. We document the histological cranial anatomy of individuals representing Monodelphis domestica, Dromiciops gliroides ...
Forasiepi, Analia Marta, Sánchez Villagra, Marcelo R.   +1 more
core   +4 more sources

Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Nance‐Horan syndrome (NHS; OMIM 302350) is a rare, X‐linked syndrome characterized by bilateral congenital cataracts leading to profound vision loss, specific dental anomalies including characteristic screwdriver blade‐shaped incisors, facial anomalies, and intellectual disability.
Maria K. Haanpää, Chad R. Haldeman‐Englert, Marja Hietala, Melisa S. Tanverdi, Patrick P. Koty, Diana Brightman, Eniolami Dosunmu, Shailja Tibrewal, Savleen Kaur, Anupriya Kaur, Raj Kumar Verma, Alejandra G. de Alba Campomanes, Virginia Utz, Anne M. Slavotinek, Cynthia Curry   +14 more
wiley   +1 more source

Schwannoma of the nasal septum-a case report [PDF]

, 2012
Schwannomas of the nasal cavity and paranasal sinuses are very rare. We report the case of a50-year-old woman with a schwannoma arising from the nasal septum.
Felix, Vinod, Janardhanan, Sunil, Kulothungan, Kulothungan   +2 more
core   +1 more source

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

Higher incidence of headache in patients with intermittent mucosal contact points between the septum and lateral nasal wall

Laryngoscope Investigative Otolaryngology, 2021
Introduction The nasal mucosal contact points between the two opposing mucosal surfaces leading to the headache had been a point of debate for many years; the intermittent and fixed contact points and their relationship with headache have never been ...
Ahmed Shaikh, Hamad Al Saey, Sara Ashkanani, Mansour Alsulaiti, Emad Alduhirat, Adham Aljariri, Maryam Abdulraheem, Shanmugam Ganesan   +7 more
doaj   +1 more source

Nasal septum mucocele in a patient with two other mucoceles of the paranasal sinuses: late complications of maxillofacial trauma [PDF]

Rhinology Online, 2020
Introduction: Mucoceles are pseudocystic lesions that, despite being benign, may cause diverse symptoms related to its expansive nature. Although their most common location in the nose is the frontoethmoidal sinuses, they can occur in other sites.
A. Fontes Lima, F. Carvalho Moreira, C. Azevedo, S. Vilarinho   +3 more
doaj   +1 more source

Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat, Marjolaine Champagne, Mathieu Bergeron, Philippe Dodin, Nadia Roumeliotis   +4 more
wiley   +1 more source