Results 141 to 150 of about 283,817 (266)

Chromosome 3q22.2‐q26.2 Interstitial Deletion in a Patient With Wisconsin Syndrome, Blepharophimosis‐Ptosis‐Epicanthus Inversus Syndrome, Dandy‐Walker Malformation, Pierre Robin Sequence, and Recurrent Infections

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 10, October 2025.
ABSTRACT Wisconsin syndrome is a very rare genetic condition characterized by coarse facies, prominent nasal tip, bushy high arched/upsweeping eyebrows, and a full/everted lower lip. Deletion of chromosome 3q24q25 region is considered critical for its manifestation.
Pankaj Prasun   +2 more
wiley   +1 more source

Persistent Ompahalomesenteric Duct in a Newborn With 16p11.2 Deletion: Report of New Findings

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Omphalomesenteric duct (OMD) is an embryologic communication between the extraembryonic yolk sac and the primitive midgut. The OMD malformations are relatively rare diseases associated with developmental defects related to the closure of the omphalomesenteric duct. These malformations can present in various forms, including cysts, fistulas, or
Surasak Puvabanditsin   +7 more
wiley   +1 more source

Gastric Volvulus, Pancreatic Volvulus, and Wandering Spleen: A Rare Emergency Triad Behind Acute Abdomen

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
Coronal and 3D reconstruction illustrating the rare triad of gastric volvulus, pancreatic volvulus, and wandering spleen, highlighting abnormal organ positions and the importance of prompt diagnosis and surgical intervention in acute abdomen. ABSTRACT Gastric volvulus is a rare but serious gastrointestinal disorder that can lead to obstructive ...
Parvaneh Layegh   +2 more
wiley   +1 more source

Sister Mary Joseph's Nodule Revealing Klatskin's Cholangiocarcinoma at the Yalgado Ouedraogo University Hospital: Case Report and Literature Review

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Umbilical cutaneous metastases of abdomino‐pelvic tumors are rare. They are known as Sister Mary Joseph nodules. The presence of this nodule indicates an advanced cancerous lesion and is associated with a poor prognosis. Because of its rarity, the Sister Mary Joseph nodule can go unnoticed.
Lawagoulé Joseph Emile Ky   +11 more
wiley   +1 more source

Incarcerated Littre’s Umbilical Hernia: A Case Report

open access: yesJournal of Nepal Medical Association
Littre’s hernia is an extremely rare type of hernia which has Meckel’s diverticulum as its content. A 63-year-old male, presented to the emergency department with chief complaints of swelling and pain around the umbilicus. The patient was diagnosed with
Binod Bade Shrestha   +4 more
doaj   +1 more source

Hydrogel Microspheres as Versatile Platforms for Biomedical Research: Design, Properties, and Applications

open access: yesMedComm, Volume 6, Issue 10, October 2025.
Schematic diagram illustrating the comprehensive landscape of hydrogel microspheres (HMs). (A) The components of HMs. (B) Preparation technologies employed in fabricating HMs. (C) The diverse applications of HMs across different fields. (D) The therapeutic applications of HMs in the treatment of various systemic diseases, demonstrating their potential ...
Meng Yang   +14 more
wiley   +1 more source

Epigastric and umbilical hernia; work relatedness and return to work.

open access: yesIranian Journal of Public Health, 2013
Abdominal wall hernia is common but reliable scientific data about its work relatedness is very limited and inconsistent. In this paper, a less common type of abdominal wall hernia in a 30 year old male worker is presented with recurrence after first ...
Ramin Mehrdad   +2 more
doaj   +2 more sources

Spontaneous rupture of umbilical hernia without ascites: A case report and literature review

open access: yesInternational Journal of Abdominal Wall and Hernia Surgery
Umbilical hernia is a common condition, but spontaneous rupture with omental evisceration, particularly in the absence of ascites or other risk factors, is extremely rare. We present a case of omental evisceration through a long-standing umbilical hernia
Razaz Aldemyati, Zaid Malaibari
doaj   +1 more source

SYNTROPY OF UNCLASSIFIED COMPLEXES OF MULTIPLE CONGENITAL MALFORMATIONS [PDF]

open access: yes, 2014
Statistical analysis of unclassified complexes multiple of congenital malformations was performed . Frequency of the most frequent combination of defects consisting of multiple congenital malformations was determined , syntropy index was defined ...
Andriichuk, D.   +3 more
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