Results 61 to 70 of about 28,505 (240)

A simple new technique for neo-umbilicoplasty [PDF]

open access: yes, 2005
A
Blondeel, Phillip   +2 more
core   +2 more sources

Tall Stature and Scoliosis Associated With a Novel Homozygous Loss‐of‐Function Missense Variant in NPR3

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT NPR3‐related tall stature is characterized by tall stature, elongated big toes, and additional epiphyses in hand and foot bones. The condition is caused by biallelic loss‐of‐function variants affecting natriuretic peptide receptor 3 (NPR3). Five individuals from four different families have been reported.
Pierre Moffatt   +4 more
wiley   +1 more source

A case of incarcerated umbilical hernia in a 9-year-old child and review article on pediatric umbilical hernia

open access: yesJournal of Pediatric Surgery Case Reports, 2022
Umbilical hernia in children is a relatively common condition with a higher prevalence in premature, low-birth weight and black children. By contrast, complicated umbilical hernia rarely occurs.
Aleksandar Stepanovski   +3 more
doaj  

Paraumbilical/Umbilical Hernia

open access: yes, 2021
Umbilical hernia is a common pathology that occurs in around 2% of the population. About 10% of abdominal hernias are umbilical hernias and umbilical hernia repair is among the most commonly performed surgeries in adults. The diagnosis is straightforward when tissues or organs such as the omentum or a bowel segment bulge out through an opening in the ...
Andrea Sanna, Luca Felicioni
openaire   +4 more sources

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, EarlyView.
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

UMBILICAL HERNIA OF THE NEWBORN [PDF]

open access: yesThe American Journal of the Medical Sciences, 1895
n ...
openaire   +2 more sources

Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Rare diseases impact approximately 1 in 10 people worldwide, and yet, less than 5% of all rare diseases currently have an approved treatment option available. This is due to many challenges unique to rare diseases, including small, diverse patient populations, the cost of drug development that is not proportionate to the number of patients who
Caleb P. Bupp   +7 more
wiley   +1 more source

Introducing Novel Surgical Clinical Correlations Into an Undergraduate Medical Anatomy Course

open access: yesClinical Anatomy, EarlyView.
ABSTRACT Anatomy education is a hallmark of many preclinical medical school curricula, but students are often unable to identify the clinical relevance of anatomy and its applications. Vertical curricula that integrate clinical concepts into the preclinical basic science years and vice versa have been shown to benefit student learning and increase ...
Liam McLoughlin   +5 more
wiley   +1 more source

Placental Transfusion for Asphyxiated Infants. [PDF]

open access: yes, 2019
The current recommendation for umbilical cord management of non-vigorous infants (limp, pale, and not breathing) who need resuscitation at birth is to immediately clamp the umbilical cord.
Bava, Sunita   +3 more
core  

Comments on Saint’s triad [PDF]

open access: yes, 2015
Yamanaka et al. described two case studies involving coexistent cholelithiasis, hiatal hernia, and umbilical hernias, and discussed clinical similarities with the classical features of the Saint’s triad.
Lister Arruda Modesto dos Santos   +1 more
core   +1 more source

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