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Congenital birthmarks: A common finding in newborns

Martins, Cátia; Correia, Laura; Ramos, Leonor; Castelo, Rui

Epidermal nevi are generally benign, isolated conditions, occurring in approximately 1 to 3 per 1,000 newborns, with sebaceous nevi accounting for approximately half of cases. The authors present two clinical cases of newborns with different subtypes of congenital epidermal nevi: a papillomatous epidermal nevus and a sebaceous nevus. Epidermal nevi typically present as a single benign lesion. However, in some c...


Acquired Torticollis in Children: A Clinical Manifestation with a Broad Spectru...

Correia, Laura; Folques, Carolina; Pais, Rui Pedro; Costa, José Augusto; Palavra, Filipe

Acquired torticollis in children is a clinical manifestation with a wide etiological spectrum, which ranges from traumatic, infectious or inflammatory processes, to non-musculoskeletal entities of neurological, tumoral or even ophthalmological origin. It can constitute the form of presentation of benign and self-limiting processes, as well as progressive and potentially fatal conditions, so the identification o...

Date: 2024   |   Origin: SINAPSE

Five years of universal newborn hearing screening: an incidence study

Leal, Bárbara; Lopes, Ana Cristina; Peixoto, Daniela; Correia, Laura; Almiro, Maria Miguel; Vilar, João; Azevedo, Luísa; Bicho, Maria Adelaide

Introduction: Universal newborn hearing screening (UNHS) is an essential tool for early diagnosis and prognosis of hearing loss. The aims of this study were to estimate the incidence of sensorineural hearing loss (SNHL) in the Baixo Vouga region, to evaluate the importance of first-degree parental consanguinity (FDPC) as a risk factor for hearing loss in the UNHS program of Centro Hospitalar do Baixo Vouga (CHB...


Teoria das Transições – Afaf Meleis

Soares, Rayana; Gouveia, Inês; Correia, Laura; Sardo, Mariana; Cardoso, Rita; Castro, Rodrigo; Loureiro, Fernanda


Parental Consanguinity and Risk for Childhood Hearing Loss: A Retrospective Coh...

Leal, Bárbara; Lopes, Ana Cristina; Peixoto, Daniela; Correia, Laura; Almiro, Maria Miguel; Vilar, João; Azevedo, Maria Luísa; Bicho, Maria Adelaide

Introduction: Genetic causes are responsible for half of the cases of hearing loss, most of them being the result of non-syndromic genetic changes resulting from autosomal recessive inheritance. Parental consanguinity might be an indicator to consider in the diagnosis of these cases. The aim of this study was to assess its importance as a risk factor for childhood hearing loss.Material and Methods: A retrospect...

Date: 2023   |   Origin: Acta Médica Portuguesa

Five years of universal newborn hearing screening: An incidence study

Leal, Bárbara; Lopes, Ana Cristina; Peixoto, Daniela; Correia, Laura; Almiro, Maria Miguel; Vilar, João; Azevedo, Maria Luísa; Bicho, Maria Adelaide

Introduction: Universal newborn hearing screening (UNHS) is an essential tool for early diagnosis and prognosis of hearing loss. The aims of this study were to estimate the incidence of sensorineural hearing loss (SNHL) in the Baixo Vouga region, to evaluate the importance of first-degree parental consanguinity (FDPC) as a risk factor for hearing loss in the UNHS program of Centro Hospitalar do Baixo Vouga (CHB...


Impact of Confinement on the Health of Children and Adolescents During the COVI...

Peixoto, Daniela; Leal, Bárbara; Ribeiro, Daniela; Correia, Laura; Hipólito, Elsa; Rocha, Paula

N/a.; N/a.

Date: 2021   |   Origin: Acta Médica Portuguesa

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