Results 91 to 100 of about 9,344 (228)

A Population‐Based Study of Limb Body Wall Complex With Proposed Features for Prenatal Diagnosis

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 11, November 2025.
ABSTRACT Limb body wall complex (LBWC) is a lethal condition comprising major congenital anomalies. Although currently diagnosed in the early prenatal period, historical diagnostic criteria are based on detailed pathological assessments. Prenatal and postnatal findings of LBWC and their phenotypic overlap with body stalk anomaly (BSA) and recurrent ...
Mary Ann Thomas   +2 more
wiley   +1 more source

A Report on the First Ex‐Utero Intrapartum Treatment (EXIT) Procedure in West Africa

open access: yesClinical Case Reports, Volume 13, Issue 11, November 2025.
The first ex‐utero intrapartum treatment (EXIT) procedure in West Africa. EXIT procedure can be done safely under resource‐constraints settings. Adverse perinatal outcomes can still occur, even after a successful EXIT procedure. ABSTRACT The Ex utero Intrapartum Treatment (EXIT) is a complex perinatal intervention designed to secure the fetal airway ...
Betty Anane‐Fenin   +16 more
wiley   +1 more source

Antenatal sildenafil administration to prevent pulmonary hypertension in congenital diaphragmatic hernia (SToP-PH): study protocol for a phase I/IIb placenta transfer and safety study

open access: yesTrials, 2018
Background Congenital diaphragmatic hernia is an orphan disease with high neonatal mortality and significant morbidity. An important cause for this is pulmonary hypertension, for which no effective postnatal therapy is available to date.
Francesca Maria Russo   +8 more
doaj   +1 more source

Neonatology. Introduction [PDF]

open access: yes, 2017
Навчальний посібник містить інформацію про основні принципи догляду за новонародженими дітьми, перехідні умови та годування немовлят, основні принципи реанімації новонароджених.
Petrashenko, Viktoriia Oleksandrivna   +11 more
core  

Recent Innovations & Daily Problems. A new prosthesis in inguinal hernia repair:preliminary results of a pilot study. [PDF]

open access: yes, 2015
Introduction: Elective surgery for inguinal hernia is affected by very low mortality « 1 per 10000 operation); in contrast, when surgery is carried out for complicated inguinal hernia, risks of postoperative complication are higher.
Agarwal, N   +102 more
core   +1 more source

Evaluating the reproductive ability of breeding rams in North-Eastern Spain using clinical examination of the body and external genitalia [PDF]

open access: yes, 2015
Background Predicting the ability of rams to detect, mate and fertilise ewes in oestrus accurately is certainly difficult; however, tests based on clinical examinations have been performed to assess the overall potential capacity of rams to serve and ...
Alabart Alvarez, José Luis   +4 more
core   +2 more sources

PENTALOGY OF CANTRELL: A CASE REPORT

open access: yesHealth Problems of Civilization
Cantrell’s pentalogy is a rare developmental disorder occurring between the 14th and 18th day of embryonic life. Diagnosis is possible in the first trimester, when the rupturing of the continuity of the anterior chest cavity and abdominal walls is ...
Justyna Płusajska   +4 more
doaj   +1 more source

Gastroschisis and omphalocele [PDF]

open access: yes, 1993
It has been widely acknowledged that exomphalos and gastroschisis are two different clinical entities. Their etiology and pathogenesis, however, remain controversial.
Molenaar, J.C., Tibboel, D. (Dick)
core   +1 more source

Prenatal Diagnosis of a Fetus with Ring Chromosomal 15 by Two- and Three-Dimensional Ultrasonography

open access: yesCase Reports in Obstetrics and Gynecology, 2014
We report on a prenatal diagnosis of ring chromosome 15 in a fetus with left congenital diaphragmatic hernia (CDH) and severe intrauterine growth restriction (IUGR).
Ingrid Schwach Werneck Britto   +8 more
doaj   +1 more source

Mucopolysaccharidosis VI

open access: yesOrphanet Journal of Rare Diseases, 2010
Mucopolysaccharidosis VI (MPS VI) is a lysosomal storage disease with progressive multisystem involvement, associated with a deficiency of arylsulfatase B leading to the accumulation of dermatan sulfate. Birth prevalence is between 1 in 43,261 and 1 in 1,
Harmatz Paul   +3 more
doaj   +1 more source

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