Results 21 to 30 of about 3,417,928 (205)

EPILEPSY MANIFESTATIONS IN PATIENTS WITH MALFORMATIONS OF THE CORPUS CALLOSUM

open access: yesЭпилепсия и пароксизмальные состояния, 2017
The article deals with epileptic manifestations with malformations of the corpus callosum of the example of two disembriogenetic syndromes (Aicardi syndrome and Pierre-Robin syndrome).
O. A. Milovanova   +3 more
doaj   +1 more source

Guiding Occlusal Delvelopment wih Functional Appliances

open access: yesAustralasian Orthodontic Journal, 1995
Orthodontic treatment with functional appliances has been available since the beginning of this century. One of the first known functional appliances, ‘the Monobloc’, was introduced at a conference in Paris in 1926 by Pierre Robin.1 This appliance had ...
Nielsen Ib Leth
doaj   +1 more source

Catel–Manzke syndrome: Further delineation of the phenotype associated with pathogenic variants in TGDS

open access: yesMolecular Genetics and Metabolism Reports, 2015
Catel–Manzke syndrome is a rare autosomal recessive disorder characterized by Pierre Robin sequence with hyperphalangy and clinodactyly of the index finger. Recently, homozygous or compound heterozygous pathogenic variants in TGDS have been discovered to
Rachel Pferdehirt   +4 more
doaj   +1 more source

Use of Mandibular Distraction Osteogenesis to Correct Micrognathia and Airway Obstruction in Newborn Female

open access: yesMarshall Journal of Medicine, 2022
We present a case of Pierre Robin sequence and Neonatal Abstinence Syndrome (NAS) in a newborn female patient to highlight the surgical technique of mandibular distraction osteogenesis to correct airway obstruction due to micrognathia.
Seneca Williams, Adam Van Horn
doaj   +1 more source

Pierre Robin sequence and keratoconus, a rare association

open access: yesIberoamerican Journal of Medicine, 2022
Pierre Robin sequence (PRS) is an inherited disorder that affects one in between 8,500 and 14,000 people and is characterized by a triad of clinical signs. These include micrognathia, glossoptosis and obstruction of the upper airway, typically associated
Jorge Hernández-Cerdá   +2 more
doaj   +1 more source

Pudendal nerve block for circumcision of pediatric patient with Pierre Robin Sequence: case report

open access: yesBrazilian Journal of Anesthesiology, 2023
Pierre Robin Sequence (PRS) is a congenital condition characterized by micrognathia, glossoptosis, and cleft palate that presents with airway obstruction and developmental delay with or without other congenital anomalies.
Munevver Kayhan   +3 more
doaj   +1 more source

A descriptive study on individuals referred to the Council of Cleft Lip and Palate of Gazi University

open access: yesActa Odontologica Turcica, 2022
Objective: To assess the demographic characteristics and to determine the cleft types, the characteristics of the syndrome and additional anomalies, and treatment needs of patients referred to Gazi University Faculty of Medicine Cleft Lip and Palate (CLP)
Şadiye BACIK TIRANK   +7 more
doaj   +1 more source

Clinical Factors Associated with the Non-Operative Airway Management of Patients with Robin Sequence

open access: yesArchives of Plastic Surgery, 2016
Background The indications for surgical airway management in patients with Robin sequence (RS) and severe airway obstruction have not been well defined.
Frank P. Albino   +6 more
doaj   +1 more source

Role of SoxE transcription factors in development and disease

open access: yesDevelopmental Dynamics, EarlyView.
Abstract Sox8, Sox9, and Sox10 arose by multiple rounds of genome duplications from a single SoxE gene in ancestral vertebrates. In this review, we will briefly discuss the molecular structure and function of SoxE transcription factors and their evolutionary origin. We will then discuss their expression, function, and developmental disorders.
Merin Lawrence, Gerhard Schlosser
wiley   +1 more source

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