Results 71 to 80 of about 940,867 (195)

Congenital goitre and respiratory distress as rare presenting features of congenital hypothyroidism in the newborns [PDF]

, 2022
In babies with congenital hypothyroidism, congenital goiter and respiratory distress (due to upper airway compression/hypothyroidism) are rarely encountered as the first presenting signs.
Makki, Khalid A.
core   +1 more source

Prevalence of Permanent Congenital Hypothyroidism in Children in Yazd Central Iran

Iranian Journal of Public Health, 2013
Background: Congenital hypothyroidism is a condition of thyroid hormone deficiency. Approximately 1 in 4000 newborn infants has a deficiency of thyroid function.
Reza Soleimanizad, Azar Rabiei, Mahtab Ordooei, Fatemeh Mirjalili   +3 more
doaj   +2 more sources

Hyperdominant Left Circumflex Artery Challenging Conventional Paradigms and Current Guideline Recommendations: A Comprehensive Literature Review and Case Series

Clinical Case Reports, Volume 14, Issue 11, November 2026.
Summary of the patient's presentation, diagnostic evaluation, treatment, and follow‐up. ABSTRACT Despite its rarity in the general population, left dominant coronary circulation with a hyperdominant left circumflex artery (LCx) has been associated with a more severe risk for ischemic and coronary artery disease. The concealment of an isolated posterior
Amirmahdi Mohammadi, Mohammad Sadegh‐Vashveshady   +1 more
wiley   +1 more source

Screening for congenital hypothyroidism in Hong Kong

, 1986
A pilot cord blood TSH screening program for congenital hypothyroidism was commenced in Hong Kong in April 1982. By April 1984, 14,411 neonates born in two hospitals were screened for this disorder.
Yeung, CY, C. Y. YEUNG, T. L. KWOK, Kwok, TL, Cheung, PT, Lin, HJ, S. Y. CHU, J. BACON‐SHONE, Chu, SY, H. J. LIN, Low, LCK, L C. K. LOW, P. T. CHEUNG, Lee, FT, Bacon-Shone, J, F. T. LEE   +15 more
core   +1 more source

Identification of Risk‐Related Prenatal Medication Exposure Profiles for Childhood Asthma Using the Bayesian Profile Regression: A Cohort Study Using the POMME Cohort

Pharmacoepidemiology and Drug Safety, Volume 35, Issue 11, November 2026.
ABSTRACT Purpose To identify prenatal medication exposure profiles associated with childhood asthma. Methods This population‐based cohort study used data from the POMME (PrescriptiOn Médicaments Mères Enfants) cohort, including 18 851 children born in the Haute‐Garonne area (France) in 2010 and 2015, and followed until 2023.
Solène Russo, Justine Bénévent, Anna‐Belle Beau   +2 more
wiley   +1 more source

Integrated Reproductive and Cytogenetic Assessment of Infertility in a Captive Jaguar (Panthera onca)

Veterinary Medicine and Science, Volume 12, Issue 6, November 2026.
Integrated reproductive and cytogenetic assessment of infertility in a captive jaguar pair identified normal chromosomal status in both individuals, whereas impaired semen quality in the male likely represents a major limiting factor for reproductive success under the observed conditions.
Marie Altmanová, Julie Strand, Kathrine Thejll Kirchhoff, Zuzana Majtánová   +3 more
wiley   +1 more source

Intelligence quotient, anxiety, and depression in congenital hypothyroid children at school age

International Journal of Preventive Medicine, 2020
Background: Many studies who evaluated the outcome of the congenital hypothyroidism (CH) screening reported some intellectual and behavioral deficit despite early diagnose and treatment.
Mitra Nekouei, Alireza Firoozfar, Dorna Kheirabadi, Sadegh Baradaran Mahdavi, Ali Talebi, Manizheh Danesh, Maryam Yahay, Mahdokht Rahimi, Laya Golshani, Gholam Reza Kheirabadi, Mahin Hashemipour   +10 more
doaj   +1 more source

Risk and outcomes of adrenal crisis in primary adrenal insufficiency: Evidence from a 24‐year nationwide cohort study

Journal of Internal Medicine, Volume 300, Issue 5, Page 675-688, November 2026.
Abstract Background Adrenal crisis is a life‐threatening emergency. Despite preventive strategies, previous reports suggest increasing incidence and substantial mortality, but robust validated data are limited. Objective To assess temporal trends in adrenal crisis incidence and identify associated risk factors.
Ann‐Elin Meling Stokland, Lars Breivik, Ingvild Dalen, Sandra Dis Steintorsdottir, Simon Kildal, Ingrid Nermoen, Kari Lima, Margrethe Svendsen, Åse Bjorvatn Sævik, Aleksandra Debowska, Stina Therese Sollid, Daniel Hannisdal, Trine Elisabeth Finnes, Agnes Judit Horvath, Elin Korsgaard, Hallvard Singsås, Bjørn O. Åsvold, Maria Eriksson Steigen, Sigrid Blika, Petya Milova, Anders Svare, Anja Fog Heen, Lene Katrine Bjerke, Marianne Stedje, Siri Carlsen, Bjørn Gunnar Nedrebø, Anders Palmstrøm Jørgensen, Grethe Å. Ueland, Marianne Øksnes, Eystein Sverre Husebye   +29 more
wiley   +1 more source

The Lupus Damage Index Revision Program: Results From the Item Generation and Reduction Phases

Arthritis Care &Research, Volume 78, Issue 10, Page 1449-1466, October 2026.
Objective A data‐driven and expert/patient consensus‐based project to develop a revised Systemic Lupus International Collaborating Clinics (SLICC)/American College of Rheumatology (ACR) Damage Index (SDI) is under way supported by SLICC, ACR, and the Lupus Foundation of America. Our objective is to report the item generation and reduction phase results
Burak Kundakci, Megan R. W. Barber, Ann E. Clarke, Sindhu R. Johnson, Anselm Mak, Hermine I. Brunner, Murat Inanc, Rosalind Ramsey‐Goldman, Guillermo Ruiz‐Irastorza, Ellen M. Ginzler, John G. Hanly, Alexandra Legge, Cynthia Aranow, Laurent Arnaud, Nathalie Costedoat‐Chalumeau, Dafna D. Gladman, Søren Jacobsen, Michelle Petri, Clovis A. Silva, Évelyne Vinet, Alexandre E. Voskuyl, SDI Revision Literature Review Groups, SDI Revision Delphi Panel, SDI Revision Item Reduction Committee, SDI Revision Clinical Domain Groups, Ian N. Bruce   +25 more
wiley   +1 more source

Defining Features of Gabriele‐de Vries Syndrome in Adults: A Case Report and Literature Review

American Journal of Medical Genetics Part A, Volume 200, Issue 10, Page 2396-2404, October 2026.
ABSTRACT Gabriele‐de Vries syndrome (GADEVS) is a neurodevelopmental disorder caused by heterozygous pathogenic variants in the YY1 gene. Like most rare genetic syndromes, the adult manifestations of GADEVS remain poorly defined. Here, we describe the oldest patient reported to date with GADEVS—a 63‐year‐old woman with a c.1177_1179del YY1 variant ...
Ethan W. Hollingsworth, Changrui Xiao
wiley   +1 more source