Results 121 to 130 of about 36,320 (252)

A massive hiatal hernia that mimics a congenital diaphragmatic hernia. An unusual presentation of hiatal hernia in childhood: Report of a case

, 2002
A massive hiatal hernia containing the colon, intestine, and stomach with organoaxial volvulus is an uncommon entity in childhood. This clinical form of a hiatal hernia may mimic congenital diaphragmatic hernia and chest pathologies.
Herek, Özkan., Yıldıran, Nergül.
core   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

Combined Long‐Read Genome and Transcriptome Sequencing Establishes Novel Variants in MEGF8 as the Cause for Carpenter Syndrome Type 2

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1719-1724, July 2026.
ABSTRACT Carpenter syndrome type 2 (CRPT2) is a rare autosomal recessive disease mainly characterized by craniosynostosis and polysyndactyly. CRPT2 is the rarer subtype of Carpenter syndrome (CRPTS) and is caused by biallelic variants in the multiple epidermal growth factor‐like domains 8 gene (MEGF8).
Kiana Rashidi, Bhavi P. Modi, Phillip A. Richmond, Massimo Mangino, Loryn Byres, Cassie McDonald, Joshua Dalmann, Simran Samra, Kate L. Del Bel, Anna Lehman, Jessica L. Zambonin, Stuart E. Turvey   +11 more
wiley   +1 more source

Congenital Middle Mesocolic Hernia: A Case Report

, 2014
Internal hernia is herniation of a viscus, usually in the small bowel, through a normal or abnormal aperture within the peritoneal cavity. Its incidence has been reported to be 1–2 per cent.
Selvaraj Karthikesh; Mahatma Gandhi Medical College & Research Institute, Sri Balaji Vidyapeeth University, Pondicherry, India, Petchiappan C Ganesh Babu; Mahatma Gandhi Medical College & Research Institute, Sri Balaji Vidyapeeth University, Pondicherry, India, Thangamani Arun; Mahatma Gandhi Medical College & Research Institute, Sri Balaji Vidyapeeth University, Pondicherry, India, Kannan Usha; Mahatma Gandhi Medical College & Research Institute, Sri Balaji Vidyapeeth University, Pondicherry, India, Mohamedhanif P Naseeruddin; Mahatma Gandhi Medical College & Research Institute,Sri Balaji Vidyapeeth University, Pondicherry, India, Narayanasamy Subbaraju Kannan; Mahatma Gandhi Medical College & Research Institute, Sri Balaji Vidyapeeth University, Pondicherry, India   +5 more
core  

Successful Cesarean Section for Dystocia due to Incomplete Cervical Dilation in a Doe: A Veterinary Case Report

Clinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Failure of cervical progression during prolonged labor should prompt early reassessment rather than repeated obstetric manipulation. In goats, persistent cervical rigidity despite ongoing uterine activity warrants timely escalation of care to avoid preventable complications in both the doe and kid, particularly in field and smallholder ...
Chukwuka Elendu, Dependable C. Amaechi, Tochi C. Elendu, Emmanuel C. Amaechi, Ijeoma D. Elendu   +4 more
wiley   +1 more source

Our Incidence of Diaphragmatic Hernia Detected with MDCT in the Past Two Years [PDF]

Düzce Tıp Fakültesi Dergisi, 2015
Aim: Diaphragmatic hernia develops as a result of extension of the intraabdominal organs to the thorax from a diaphragmatic defect which may be either a congenital fusion defect or subsequently formed defect(iatrojenic or traumatic).
Nesrin Atcı, Hanifi Bayaroğulları, Sibel Doğru, Ramazan Davran   +3 more
doaj  

Congenital diaphragmatic hernia

, 2021
Boonthai, Ampaipan, Losty, Paul D
openaire   +1 more source

WWOX Mutation as a Rare Cause of Neonatal‐Infantile Parkinsonism Mimicking a Neurotransmitter Disorder: A Case Report

Journal of Paediatrics and Child Health, EarlyView.
Ozge Serce Pehlevan, Gizem Gider Yaman, Anıl Gok, Leman Tekin Orgun   +3 more
wiley   +1 more source

The Safety of Treating Women With Inflammatory Bowel Disease With Allopurinol and Low‐Dose Thiopurine During Pregnancy: A Single‐Center Experience

JCC Plus, Volume 1, Issue 4, July 2026.
ABSTRACT Background Low‐dose thiopurine therapy in combination with allopurinol (LD‐THIO/ALLO) is a widely used treatment for inflammatory bowel disease (IBD). However, little is known about the effects of in utero exposure to this combination on pregnancy and birth outcomes.
Kavitha Sivananthan, Signe Wildt, Marianne Kiszka‐Kanowitz, Gitte Pedersen, Ida Vind, Inge Nordgaard‐Lassen, Andreas Munk Petersen, Johan Burisch, Helle Kristensen, Klaus Theede   +9 more
wiley   +1 more source

Congenital Diaphragmatic Hernia: Atypical Early X-Ray Presentation

, 2014
Congenital Diaphragmatic Hernia (CDH) is a congenital malformation of the diaphragm that allows herniation of the abdominal organs into the thoracic cavity. The most common type of CDH is Bochdalek Hernia. It is seen commonly on the left side than right,
Kumar Srivastava, Shashank, A. Wasey, Waiz   +1 more
core   +1 more source