Results 241 to 250 of about 2,203,451 (295)

Distinguishing Between Innocent and Pathologic Pediatric Heart Murmurs: A Case Report. [PDF]

Cureus
Thomas KI.
europepmc   +1 more source

The Legal Status of Conjoined Twins in Islamic Law: A Socio‐Legal Analysis

Sociology Lens, EarlyView.
ABSTRACT Conjoined twins are a rare congenital anomaly. Conjoined twins can occur in various morphological types. Conjoined twins are perceived not only as a physical difference but also as a subject of interest and curiosity in many areas of society.
Merve Yiğitoğlu
wiley   +1 more source

Expansion of the Phenotypic and Genotypic Spectrum of MED13L-Associated Neurodevelopmental Disorder: A Case Report and Literature Review. [PDF]

Mol Genet Genomic Med
Wang Z, Chen X, Cui Z, Qi X, Gu L, Liu Y, Zhao W, Jiang Y.   +7 more
europepmc   +1 more source

Recent advances in polyendocrine metabolic ovarian syndrome, formerly polycystic ovary syndrome, with emphasis on endocrine and metabolic dysfunction and cardiovascular risk

Journal of Internal Medicine, EarlyView.
Abstract Polyendocrine metabolic ovarian syndrome (PMOS), previously known as polycystic ovary syndrome, affects 10%–13% of women of reproductive age and remains underdiagnosed despite its substantial health burden. The introduction of the new PMOS nomenclature in 2026 reflects a fundamental shift in understanding the condition as a lifelong endocrine ...
Maria Forslund, Johanna Melin, Anju E. Joham, Terhi T. Piltonen, D. Aled Rees, Helena J. Teede   +5 more
wiley   +1 more source

Functional genomics in <i>Xenopus</i> identifies ARHGAP10 as a congenital heart disease and ciliopathy gene. [PDF]

iScience
Sochacka E, Hinson ST, Shook DR, DeSimone DW, Kulkarni SS.   +4 more
europepmc   +1 more source

Treat, Reassess, Repair: Redefining Operability in Pulmonary Arterial Hypertension Associated With Atrial Septal Defect. [PDF]

JACC Case Rep
Cramer JW.
europepmc   +1 more source

Case Report: A rare stop-gained <i>MYZAP</i> mutation is associated with atrioventricular septal defects in an Arabian family. [PDF]

Front Cardiovasc Med
Zaher Z, Abdelmohsen G, Bahaidarah S, Baamer F, Abdulrhman Abdulkareem A, Alrefaei AF, Naseer MI, Abu-Elmagd M.   +7 more
europepmc   +1 more source

Global research trends in heterotaxy syndrome with congenital heart defects: a 20-year bibliometric analysis (2006-2025). [PDF]

Transl Pediatr
Zhao M, Cong X, Liu X, Pan J, Hou Z, Wang F, Wang L.   +6 more
europepmc   +1 more source

Clinical and Genetic Profile of One Molecularly Confirmed and One Clinically Suspected Case of LZTR1 -Related Noonan Syndrome. [PDF]

Clin Genet
Skrzyńska K, Kalina-Faska B, Błaszczyk E, Gawlik-Starzyk A.   +3 more
europepmc   +1 more source