Results 61 to 70 of about 557 (164)

Hábitos bucales deformantes asociados al micrognatismo transversal en escolares [PDF]

Introduction: Transverse micrognathia is an anomaly that affects the transverse development of the maxilla and is considered one of the fundamental morphopathological causes of dental malocclusions.
Roca Jerez , Daniel, Reyes Reyes, Eduardo Salvador, Torres Vargas , Lais de la Caridad, Jorge Enamorado , Elaine Suleidis, Enamorado Piña, Gertrudis Valentina, Alarcón Vázquez , Deysy Arlety   +5 more
core   +1 more source

Caracterización de la retención de caninos maxilares en pacientes pediátricos de Ciego de Ávila [PDF]

Introduction: We report findings that allow us to observe the impacted maxillary canine as an entity of important prevalence. In the province of Ciego de Avila there is little research published on this eruptive alteration.Objectives: To describe ...
Espinosa Morales, Luxury, Hernández González, Leonor de las Mercedes, San Miguel Pentón, Armando, Blanco Ruíz, Yordania, León Alfonso, José, Roque Morgado, Maikel   +5 more
core  

Expanding Spectrum of FIG4-Related Neurological Disorders of Lysosomal Homeostasis: Case Report and Overview of the Potential Genotype-Phenotype Correlations. [PDF]

Clin Genet
Prasun P, Rasberry M.
europepmc   +1 more source

Beyond Snoring: Unexpected Presentation of Obstructive Sleep Apnea. [PDF]

Cureus
Vieira PM, Aranda AC, Martins FAC, Ferreira IA, Barroso M, Khomynets M.   +5 more
europepmc   +1 more source

Mandibular cephalometric characteristics in children from 8 to 12 years old with unilateral cleft lip and palate who attended the craniofacial malformation program of FISULAB in the period 2010 to 2017, phase I

, 2018
Describir las características cefalométricas mandibulares en pacientes con labio paladar hendido unilateral completo (LPHU) entre los 8 y los 12 años asistentes al programa de malformaciones de la Universidad El Bosque y compararlas con los parámetros de
Pulido Otalvaro, Mònica Andrea
core  

Congenital Syngnathia With Holoprosencephaly: A Case Report of a Fatal Presentation in a Resource-Limited Setting. [PDF]

Clin Case Rep
Haile AM, Mengistie BT, Tamiru TY, Mengistie CT, Abebe DG, Haile BM.   +5 more
europepmc   +1 more source

A de novo SOX11 mutation causing hypogonadotropic hypogonadism: a case report and literature review. [PDF]

BMC Pediatr
Chu S, Yuan X, Niu Q, Gu W.
europepmc   +1 more source

Impaired IFN-γ-mediated innate and adaptive immunity in Coffin-Siris syndrome type 2: immunological insights from a patient with a recurrent <i>ARID1A</i> mutation. [PDF]

Front Immunol
Peng Q, Yang Y, Zhang Y, Li S, Zhong B, Luo Q, Lu X.   +6 more
europepmc   +1 more source

Expanding the Phenotypic Spectrum Associated With Loss-of-Function SMARCA4 Variants to Eye Developmental Anomalies. [PDF]

Clin Genet
Chesneau B, Willems M, Bouazzaoui A, Lequeux L, Plaisancié J, El Chehadeh S, Dollfus H, Chassaing N.   +7 more
europepmc   +1 more source

Beyond Neurodevelopmental Delay: BICRA-Related Coffin-Siris Syndrome 12 with Severe Intestinal Dysmotility and Recurrent Pneumothorax. [PDF]

Genes (Basel)
Wang H.
europepmc   +1 more source