Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters











Database
Language
Publication year range
1.
Am J Med Genet A ; 185(8): 2356-2360, 2021 08.
Article in English | MEDLINE | ID: mdl-34047053

ABSTRACT

Down syndrome (DS) is the most common chromosomal condition. Anatomical and functional variations in the upper and lower airways are component manifestations of the syndrome and increase the risk of various medical problems. The objective of this study was to determine the prevalence of otorhinolaryngological and respiratory diseases in a DS outpatient clinic over a 3-year period. Medical records data from 1207 patients were retrospectively reviewed. Newborn Hearing Screening was positive in 7.1% of patients. Brainstem auditory evoked potential was performed in 1101 children and showed a hearing loss of 19.8% in the first year. It was positive in 21% of 1021 exams. Audiometry was altered in 64 of 994 exams (6.4%), showing a conductive loss in 90%. Adenotonsillectomy was performed in 308 (25.5%) patients, and 169 (14.0%) required serous otitis ventilation tubes. Asthma was observed in 140 (11.6%) patients, and allergic rhinitis in 544 (56.6%). There were hospitalizations for invasive infection in 480 (39.8%) children, and two (0.2%) patients had severe septicemia from pulmonary focus. Five (0.4%) infants had laryngotracheomalacia, and one patient had anomalous right tracheal bronchus. Recognizing the prevalence of respiratory and otorhinolaryngological disorders in patients with DS allows the promotion of optimal follow-up and early treatment, preventing the development of sequelae.


Subject(s)
Down Syndrome/complications , Down Syndrome/epidemiology , Otorhinolaryngologic Diseases/complications , Otorhinolaryngologic Diseases/epidemiology , Respiratory Tract Diseases/complications , Respiratory Tract Diseases/epidemiology , Adolescent , Adult , Brazil/epidemiology , Child , Child, Preschool , Female , Humans , Male , Middle Aged , Otorhinolaryngologic Diseases/diagnosis , Prevalence , Public Health Surveillance , Respiratory Tract Diseases/diagnosis , Retrospective Studies , Young Adult
2.
Am J Med Genet A ; 182(11): 2641-2645, 2020 11.
Article in English | MEDLINE | ID: mdl-32945116

ABSTRACT

Down syndrome is the most common chromosomal disorder, affecting 1/700 live births. Among the clinical findings, one constant concern is the high prevalence of visual disorders that, if left untreated, can negatively affect child development. The aim of this study was to determine the prevalence of ophthalmological findings among patients who attended an outpatient clinic for patients with Down syndrome in southern Brazil between 2005 and 2016. A cross-sectional study including 1,207 patients medical records were done, which 492 (40.8%) had some ophthalmological disorder. These data were subjected to descriptive analysis using Statistica software. Among the 492 patients with any ophthalmological disease, the need for glasses was found in 434 (36%) patients, keratoconus in 254 (42.1%), congenital cataract in 27 (15.1%), nasolacrimal duct obstruction in 25 (2.0%), strabismus in 22 (1.9%), nystagmus in four (0.3%), and juvenile cataract in two (0.2%). Two young adults with keratoconus underwent corneal transplantation. Although the prevalence of an ophthalmological disease among the present sample (40.8%) was lower than described in the current literature, it still reinforced the importance of routine and early evaluations in infants. These should begin at 6 months of age and be repeated half-year until 2 years old, annually until 7 years old, biennial in adolescents, and triennial in adults and elderly. Our findings of a high frequency of keratoconus support a detailed corneal study in such patients for early detection and treatment.


Subject(s)
Down Syndrome/diagnosis , Eye Diseases/diagnosis , Lacrimal Duct Obstruction/diagnosis , Adolescent , Adult , Brazil/epidemiology , Cataract/complications , Child , Child, Preschool , Cross-Sectional Studies , Down Syndrome/complications , Eye Abnormalities/complications , Eye Diseases/complications , Female , Humans , Infant , Infant, Newborn , Keratoconus/complications , Lacrimal Duct Obstruction/complications , Male , Nystagmus, Congenital/complications , Retrospective Studies , Software , Strabismus/complications , Young Adult
SELECTION OF CITATIONS
SEARCH DETAIL