Results 171 to 180 of about 572,077 (339)

A triplet pregnancy after in vitro fertilization is a procedure-related complication that should be prevented by replacement of two embryos only

, 1997
Jan Roest, Arne M. van Heusden, Arie Verhoeff, Harold V.H. Mous, G. H. Zeilmaker   +4 more
openalex   +1 more source

GATA3 Deletion Associated With Juvenile Idiopathic Arthritis: Expanding the Phenotypic Spectrum of Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Hypoparathyroidism, sensorineural deafness, and renal dysplasia (HDR) syndrome is caused by pathogenic variants in the GATA3 gene located on chromosome 10p14. Here we present a 10‐year‐old girl with HDR syndrome who also has oligoarticular juvenile idiopathic arthritis (JIA).
Lauren N. Meiss, Amanda V. Karam, Julia Shalen, David E. Tunkel, Belina Y. Yi, Kelsey S. Guthrie, Emily M. Kudalkar, Anna E. Patrick, Sonja A. Rasmussen   +8 more
wiley   +1 more source

Heat spells and birth and peripartum pregnancy complications in Germany: a scoping review. [PDF]

Arch Gynecol Obstet
Raab A, Schmitz D.
europepmc   +1 more source

Hyperparathyroidism Complicating Pregnancy [PDF]

Proceedings of the Royal Society of Medicine, 1969
openaire   +2 more sources

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source

Hyperemesis in Pregnancy: Complications and Treatment. [PDF]

Med Sci (Basel)
Gerede A, Stavros S, Moustakli E, Potiris A, Orgianelis I, Zikopoulos A, Drakakis P, Domali E, Eleutheriades M, Nikolettos N.   +9 more
europepmc   +1 more source

Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat, Marjolaine Champagne, Mathieu Bergeron, Philippe Dodin, Nadia Roumeliotis   +4 more
wiley   +1 more source

Preliminary Post-Dobbs Trends in Emergency Department Use for Early Pregnancy Complications. [PDF]

West J Emerg Med
Ager EE, Wang R, Benson LS.
europepmc   +1 more source

Long‐Read Genome Sequencing Establishes Biallelic Pathogenic Variants in DNM1 With Distinct Functional Effects as the Cause of Early Infantile Developmental and Epileptic Encephalopathy

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous de novo and inherited biallelic pathogenic variants in DNM1 have been reported in association with autosomal dominant (AD) and autosomal recessive (AR) developmental and epileptic encephalopathy, respectively, due to aberrant dynamin function or expression, with each inheritance pattern associated with a different mechanism of ...
Andy Drackley, Merlene Peter, Heba H. Akbari, Jelena Ivanisevic, Alexander Ing, Kelly Regan‐Fendt, Patrick McMullen, Kai Lee Yap   +7 more
wiley   +1 more source

The role of oral dysbiosis in pregnancy complications: a systematic review and meta-analysis of preterm birth. [PDF]

J Oral Microbiol
García-Rios P, Rodríguez-Lozano FJ, González-Murcia R, Murcia L, Victoria-Montesinos D, García-Muñoz AM.   +5 more
europepmc   +1 more source