Results 1 to 10 of about 104,773 (248)

Operative Management of Neonatal Lymphatic Malformations: Lesson Learned From 57 Consecutive Cases

open access: yesFrontiers in Pediatrics, 2021
Aim of the study: Lymphatic malformations (LMs) are rare entities, sometimes difficult to treat, that may be life-threatening when intricately connected to airway structures.
Marianna Scuglia   +14 more
doaj   +1 more source

Benign skin disease with pustules in the newborn [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2016
: The neonatal period comprises the first four weeks of life. It is a period of adaptation where the skin often presents several changes: transient lesions, resulting from a physiological response, others as a consequence of transient diseases and some ...
Flávia Pereira Reginatto   +2 more
doaj   +2 more sources

Endocrine Disorders in a Newborn with Heterozygous Galactosemia, Down Syndrome and Complex Cardiac Malformation: Case Report

open access: yesMedicina, 2023
Down syndrome is the most common chromosomal abnormality diagnosed in newborn babies. Infants with Down syndrome have characteristic dysmorphic features and can have neuropsychiatric disorders, cardiovascular diseases, gastrointestinal abnormalities, eye
Ioana Rosca   +8 more
doaj   +1 more source

Rapidly involuting congenital hemangioma [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2017
: Rapidly involuting congenital hemangioma is a rare vascular tumor that generally has a good prognosis. The authors describe a case of a newborn girl with a left cervical vascular lesion.
Susana Brás   +2 more
doaj   +2 more sources

Gastrointestinal Emergencies in Neonates: What We Should Know

open access: yes대한영상의학회지, 2020
Newborn gastrointestinal tract emergency diseases include various disorders that occur anywhere along the digestive tract. Most of them are congenital malformations, not acquired diseases.
Hyun-Hae Cho, So Mi Lee, Sun Kyoung You
doaj   +1 more source

Congenital hyperextension deformity of the knees due to arthrogryposis multiplex congenita? Case report

open access: yesCase Reports, 2020
Introduction: Arthrogryposis multiplex congenita is a disorder characterized by non-progressive joint contractures. It has an estimated prevalence of 1 in every 3 000-5 000 live births, with the same male-to-female ratio. Case presentation: This is the
Paola Andrea Romero-Campiño   +4 more
doaj   +1 more source

Niemann-Pick Disease Type C Diagnosed Using Neonatal Cholestasis Gene Panel

open access: yesThe Korean Journal of Gastroenterology, 2021
Niemann-Pick disease type C (NPC) is a neurovisceral lysosomal storage disorder caused by mutations in the NPC1 and NPC2 genes. These mutations cause the accumulation of unesterified cholesterol and other lipids in the lysosomes.
Sun Woo Park   +5 more
doaj   +1 more source

Clinical and epidemiological characterization of newborns with necrotizing enterocolitis

open access: yesABCS Health Sciences, 2022
Introduction: Necrotizing enterocolitis (NEC) is a severe inflammatory disorder that can affect the whole gastrointestinal system, particularly the ileum, and is a major cause of morbidity in premature infants.
Ariane Mendonça Neves de França   +5 more
doaj   +1 more source

Neonatal Screening on Tandem Mass Spectrometry as a Powerful Tool for the Reassessment of the Prevalence of Underestimated Diseases in Newborns and Their Family Members: A Focus on Short Chain Acyl-CoA Dehydrogenase Deficiency

open access: yesInternational Journal of Neonatal Screening, 2020
Early detection of disabling diseases, prior to clinical manifestations, is the primary goal of newborn screening (NS). Indeed, the required number of core and secondary conditions selected for screening panels is increasing in many countries ...
MariaAnna Messina   +5 more
doaj   +1 more source

Exanthematous Disease in Newborn Infants.

open access: yesThe KITAKANTO Medical Journal, 1999
生後1ヶ月未満で発疹を認め, かつ体温異常, CRP弱陽性, 血小板減少の3つの条件のいずれかを認めることを診断基準とした新生児期発疹性疾患症例20例について臨床的検討を行った.対象の在胎週数は29-40週, 出生体重は1,084-3,320gであった.血小板数が経過中15×104/μl以下となっていたのは19例であった.7例でCRPが1.0mg/dl以上に上昇していた.細菌培養ではメチシリン耐性黄色ブドウ球菌 (MRSA) が6例で咽頭もしくは便から分離された.ウイルス分離を行った18例中1例でコクサッキーB4型ウイルスが分離された.近年, 本疾患の原因としてMRSAが産生する toxic shock syndrome toxin 1 (TSST-1) が報告されているが ...
Kenichi Maruyama, Takenobu Koizumi
openaire   +2 more sources

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