Results 51 to 60 of about 1,076 (159)

Adult idiopathic hypertrophic pyloric stenosis

Journal of the Formosan Medical Association, 2015
Idiopathic hypertrophic pyloric stenosis (IHPS) is a predominantly infantile disease. The adult type of IHPS is extremely rare but it has been well recognized since the 19th century.
Hsien-Ping Lin, Yu-Chiang Lin, Chen-Yun Kuo   +2 more
doaj   +1 more source

Laparoscopic pyloromyotomy: Lessons learnt in our first 101 cases

Journal of Indian Association of Pediatric Surgeons, 2014
Aim: To analyze our experience with laparoscopic pyloromyotomy for infantile hypertrophic pyloric stenosis for the lessons that we learnt and to study the effect of learning curve.
Abhilasha Tej Handu, Vinay Jadhav, J Deepak, Jayalaxmi S Aihole, Gowrishankar, M Narendrababu, S Ramesh, K R Srimurthy   +7 more
doaj   +1 more source

Antenatal Ultrasound Findings from a Fetus that was Ultimately Diagnosed with Pyloric Stenosis in the Mid Neonatal Period: A Case Report

Gynecology Obstetrics & Reproductive Medicine, 2013
Infantile hypertrophic pyloric stenosis is the most common surgical cause of vomiting in infants. The pyloric muscle is hypertrophied and the pyloric channel becomes narrow and elongated, causing gastric outlet obstruction.
Işık Üstüner, Emine Seda Güvendağ Güven, Evren Üstüner, Ebru Düşünceli Atman, Figen Kır Şahin   +4 more
doaj  

Postoperative ultrasonography changes of the pylorus in infants with hypertrophic pyloric stenosis

The Egyptian Journal of Radiology and Nuclear Medicine, 2014
Infantile hypertrophic pyloric stenosis (IHPS) is a common condition affecting infants. Ramstedt pyloromyotomy procedure remains the standard of surgical treatment of IHPS till today.
Mohamed A. Eltomey, Hisham Almohamady Ghareeb   +1 more
doaj   +1 more source

Identification of Genetic Variants in Status Epilepticus Associated With Fever

Brain and Behavior, Volume 15, Issue 2, February 2025.
The detection rate of genetic variants was lower in patients with status epilepticus associated with fever (SEF) (4/15; 26.7%) than in those with DEE (17/27 63.0%). DEE revealed a wide variety of causative genes (16 different genes), whereas in SEF cases, only SCN1A variants were detected. SEF and DEE may have different onset mechanisms.
Hiroaki Hanafusa, Hiroshi Yamaguchi, Naoya Morisada, Ming Juan Ye, Shizuka Oikawa, Shoichi Tokumoto, Masahiro Nishiyama, Kandai Nozu, Hiroaki Nagase   +8 more
wiley   +1 more source

Infantile Hypertrophic Pyloric Stenosis [PDF]

Yeungnam University Journal of Medicine, 1996
Infantile hypertrophic pyloric stenosis(IHPS), which occurs three of 1,000 live births, is a major cause of nonbilious vomiting of early infancy but its etiology and pathogenesis are still obscure. The operation of pyloromyotomy as described by Ramstedt in 1912 remains the standard of care for the treatment of IHPS.
Young Soo Huh, Gyu Rag Kim, Son Moon Shin   +2 more
openaire   +1 more source

Efficacy of Medical Treatment for Infantile Hypertrophic Pyloric Stenosis: A Meta-analysis

Pediatrics and Neonatology, 2016
Infantile hypertrophic pyloric stenosis (IHPS) is a common disease in infancy. Pyloromyotomy is universally considered the treatment for IHPS; however, oral or intravenous atropine has been reappraised for the treatment of IHPS in the past 20 years.
Shu-Fen Wu, Hsiang-Yu Lin, Fu-Kuei Huang, An-Chyi Chen, Bai-Horng Su, Chia-Ing Li, Hung-Chih Lin   +6 more
doaj   +1 more source

Gastric outlet obstruction in an 11‐year‐old girl: A case report

JPGN Reports, Volume 5, Issue 2, Page 148-151, May 2024.
Abstract Pyloric stenosis commonly affects infants and rarely causes gastric outlet obstruction in adolescents and older children. We present the case of an 11‐year‐old girl with a 2‐month history of recurrent postprandial vomiting and weight loss. On physical examination, the patient presented with abdominal distension.
Ana Sofia Figueiredo, Carolina Soares‐Aquino, Rita Amorim, Lina Melão, Céu Espinheira, Isabel Pinto Pais, Miguel Campos, Eunice Trindade   +7 more
wiley   +1 more source

Prenatal and infantile diagnosis of craniosynostosis in individuals with RASopathies

American Journal of Medical Genetics Part A, Volume 194, Issue 2, Page 195-202, February 2024.
Abstract Fetuses with RASopathies can have a wide variety of anomalies including increased nuchal translucency, hydrops fetalis, and structural anomalies (typically cardiac and renal). There are few reports that describe prenatal‐onset craniosynostosis in association with a RASopathy diagnosis.
Carolyn R. Serbinski, April Vanderwal, Sarah E. Chadwell, Ana Isabel Sanchez, Robert J. Hopkin, Robert B. Hufnagel, K. Nicole Weaver, Carlos E. Prada   +7 more
wiley   +1 more source

Prevalence of Maxillary and Mandibular Frenal Attachment and Its Association with Age, Gender, and Oral Hygiene Status in Nepalese Population Seeking Dental Treatment

International Journal of Dentistry, Volume 2024, Issue 1, 2024.
Objective. Frenum attachments are folds of mucous membrane that connect the lips to the alveolar mucosa and underlying periosteum. Aberrant positioning of the maxillary and mandibular labial frenum can lead to various clinical issues, including mucogingival problems and midline diastema.
Arjun Hari Rijal, Manoj Humagain, Simant Lamichhane, Pratistha Ghimire, Sachita Thapa, Sivakumar Nuvvula   +5 more
wiley   +1 more source