Results 21 to 30 of about 419 (109)

Children’s Interstitial and Diffuse Lung Diseases (ChILD) in 2020

open access: yesChildren, 2020
The term children interstitial lung diseases (chILD) refers to a heterogeneous group of rare diseases that diffusely affect the lung. ChILD specific to children younger than 2 years of age include diffuse developmental disorders, growth abnormalities ...
Valentina Agnese Ferraro   +3 more
doaj   +1 more source

It Is Time to Get to Know the Neuroendocrine Cell Hyperplasia of Infancy. [PDF]

open access: yesClin Respir J
Neuroendocrine cell hyperplasia of infancy (NEHI) is a common form of childhood interstitial lung disease. A high‐resolution CT scan is a useful and major imaging approach for assisting in diagnosis. The major characteristics of NEHI on CT are the presence of typical ground glass opacities and air trapping.
Jin L, Wei W.
europepmc   +2 more sources

Subpleural pulmonary cysts in children: Associations beyond Trisomy 21

open access: yesPediatric Pulmonology, Volume 58, Issue 12, Page 3498-3506, December 2023., 2023
Abstract Background Small air‐filled peripheral subpleural cysts are a well‐described feature of pulmonary anatomy at computerized tomographic (CT) scan in children with Trisomy 21, yet only anecdotally described in association with other pathologies. The significance of these cysts is unknown.
Anuradha Singh   +5 more
wiley   +1 more source

Variants in FGF10 cause early onset of severe childhood interstitial lung disease: A detailed description of four affected children

open access: yesPediatric Pulmonology, Volume 58, Issue 11, Page 3095-3105, November 2023., 2023
Abstract Introduction Fibroblast growth factor 10 (FGF10) is a signaling molecule with a well‐established role for lung branching morphogenesis. Rare heterozygous, deleterious variants in the FGF10 gene are known causes of the lacrimo‐auriculo‐dento‐digital (LADD) syndrome and aplasia of lacrimal and salivary glands.
Katharina Schütz   +17 more
wiley   +1 more source

Respiratory distress in a 2-month-old infant: Is the primary cause cardiac, pulmonary or both?

open access: yesRespiratory Medicine Case Reports, 2018
A 2-month-old female with worsening cough, respiratory distress and an abnormal chest X-ray was referred to our institution for further evaluation of suspected scimitar syndrome.
Nadir Demirel   +5 more
doaj   +1 more source

Myxedema Coma and Acute Hepatopathy in a Dog with Severe Atherosclerosis

open access: yesCase Reports in Veterinary Medicine, Volume 2021, Issue 1, 2021., 2021
A 9‐year‐old male intact mixed‐breed dog was presented to The Ohio State University Veterinary Medical Center for evaluation of two days’ duration of weakness, lethargy, inappetence, and one episode of vomiting the day of presentation. On presentation, the dog was depressed and tetraparetic. He was noted to be icteric and dehydrated.
Leah C. Giralico   +4 more
wiley   +1 more source

Death of a Severe Underweight Infant with Pulmonary Interstitial Glycogenosis [PDF]

open access: yesKorean Journal of Legal Medicine, 2012
Pulmonary interstitial glycogenosis (PIG) is a very rare interstitial lung disease in infants. It is poorly understood, but its pathological features are distinct; they include uniform alveolar septal thickening, caused by a group of oval to spindle-shaped cells containing abundant glycogen, without apparent inflammation or fibrosis.
Seon Jung Jang   +3 more
openaire   +1 more source

Clinical assessment of heartworm‐infected Beagles treated with a combination of imidacloprid/moxidectin and doxycycline, or untreated

open access: yesJournal of Veterinary Internal Medicine, Volume 34, Issue 5, Page 1734-1745, September 2020., 2020
Abstract Background Administration of moxidectin topically and doxycycline PO has been utilized experimentally as an alternative treatment for heartworm disease. However, clinical effects of this protocol remain poorly characterized. Objective To evaluate the clinical and postmortem findings associated with administration of doxycycline and monthly 10%
Molly D. Savadelis   +9 more
wiley   +1 more source

Unusual Presentation of Pulmonary Interstitial Glycogenosis: A Case Report Study

open access: yesJournal of Comprehensive Pediatrics, 2021
Introduction: Pulmonary interstitial glycogenosis (PIG) is a kind of children’s interstitial lung disease (ChILD). This is exclusively limited to neonates and infants. Often, PIG is diagnosed in the lung biopsy in a short time after birth (usually < 6 months). Most cases of PIG in infants are symptomatic within the first days to weeks of life.
Negarin Seyyedirad   +2 more
openaire   +2 more sources

An Infant with Persistent Respiratory Failure Associated with Refractory Pulmonary Hypertension: Pulmonary Interstitial Glycogenosis

open access: yesJournal of Child Science, 2022
AbstractPulmonary interstitial glycogenosis (PIG) is a disease of unknown etiology. It is part of the interstitial lung diseases, corresponding to the compartment of the fetal pulmonary interstitium. It typically presents within the first week of life as refractory respiratory distress with tachypnea and persistent hypoxemia, and it is not associated ...
Gianfranco Tomarelli   +3 more
openaire   +1 more source

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