Results 91 to 100 of about 172,842 (350)

Ramsay Hunt syndrome a case report and review of literature [PDF]

, 2013
This is a case report of a rather rare disorder i.e. Ramsay Hunt syndrome.  This is caused by Varicella zoster infections involving geniculate ganglion of facial nerve.  This syndrome is manifested by the presence of blebs in the external auditory canal,
Thiagarajan, Balasubramanian
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

Objective preclinical measures for bone conduction implants

Frontiers in Neuroscience
The study evaluates the accuracy of predicting intracochlear pressure during bone conduction stimulation using promontory velocity and ear canal pressure, as less invasive alternatives to intracochlear pressure.
Irina Wils, Alexander Geerardyn, Alexander Geerardyn, Tristan Putzeys, Tristan Putzeys, Guy Fierens, Guy Fierens, Guy Fierens, Kathleen Denis, Nicolas Verhaert, Nicolas Verhaert   +10 more
doaj   +1 more source

A case of human acute otoacariasis caused by Rhizoglyphus sp, the first report from Iran

Journal of Acute Disease, 2018
Otoacariasis is the presence of ticks and mites in the auditory canal. A 50-year-old Iranian man was subjected at the an ear, nose, and throat clinic at Rouhani Hospital in Babol with complaint of left ear pain.
Keivan Kiakojouri, Saeid Mahdavi Omran, Ramazan Rajabnia, Abazar Pournajaf, Mojtaba Taghizadeh Armaki, Mohsen Karami   +5 more
doaj   +1 more source

Ecology of Haemaphysalis wellingtoni in Red Junglefowl [PDF]

, 2012
The ecology of the parasitic stages of Haemaphysalis wellingtoni was studied in 30 Red Junglefowls in a farm in Jenderam Hulu, Sepang, Selangor, Malaysia.
Babjee, Shaik Mohamed Amin, Nadri, Nurul Aizzati, Sabri, Jasni   +2 more
core  

First Natural Endocranial Cast of a Fossil Snake (Cretaceous of Patagonia, Argentina) [PDF]

, 2017
In this study, we describe a natural endocranial cast included in a partially preserved medium‐sized skull of the Upper Cretaceous South American snake Dinilysia patagonica.
Albino, Adriana Maria, Dozo, Maria Teresa, Trivino, Laura Natalia, Williams, Jorge Daniel   +3 more
core   +2 more sources

Clinical Presentation of the Longest Reported Living Individual With Bent Bone Dysplasia—FGFR2‐Related

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The FGFR2 gene, encoding the FGFR2 protein, plays a crucial role in embryonic cell development, particularly in bone tissue. Bent Bone Dysplasia (BBD), FGFR2‐related (MIM# 614592), is a rare severe skeletal dysplasia characterized by craniofacial differences, reduced bone mineral density, and bowed long bones.
Cheyenne Bates, Pardeep Gill, Matthew Choi, Frances Mahon, Blake Yarascavitch, Audrey Lim, Resham Ejaz   +6 more
wiley   +1 more source

Subharmonics and Auditory Nerve Tuning Curves in Gerbil [PDF]

, 2010
In the literature, an auditory nerve tuning curve obtained from single unit recording typically has a tail and a tip. Responses beyond the tip in the well supra-CF frequency region had never been documented.
Dong, Wei, Huang, Stanley, Olson, Elizabeth S.   +2 more
core   +2 more sources

Body temperature measurement uncertainty arising from ear canal geometry and temperature gradients

, 2022
Pablo Castro, G. Machin
openalex   +1 more source

KDM2B‐Related Neurodevelopmental Disorder A Case‐Series Supporting the CxxC Domain Phenotype With Emphasis on Ocular and Dermatologic Features

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The KDM2B‐related neurodevelopmental disorder is a recently identified Mendelian disorder of the epigenetic machinery associated with pathogenic variants in KDM2B. Global developmental delay, intellectual disability, congenital anomalies, and systemic manifestations characterize the disorder.
Adriana Gomes, Álvaro Martín‐Rodríguez, Miguel Del Campo, Lynne M. Bird   +3 more
wiley   +1 more source