Results 1 to 10 of about 5,862 (196)

Congenital nonsyndromic anonychia of toes due to amniotic bands

open access: yesIndian Journal of Paediatric Dermatology, 2023
Abanti Bagchi   +4 more
doaj   +1 more source

Amniotic Band Sequence [PDF]

open access: yesAmerican Journal of Obstetrics and Gynecology, 2019
Manisha, Gandhi   +2 more
openaire   +2 more sources

Fetal volvulus presenting with In utero bilious emesis: A case report

open access: yesJournal of Pediatric Surgery Case Reports
Introduction: We report a case of fetal volvulus presenting with meconium-stained amniotic fluid, illustrating how meconium can mask in utero bilious emesis.
Felix Richter   +4 more
doaj   +1 more source

AMNIOTIC BAND SYNDROME [PDF]

open access: yesMedical Journal Armed Forces India, 2001
R, Pant, H, Singh, G, Narula
openaire   +2 more sources

Body Stalk Anomaly

open access: yesDiagnostics
Abdominal wall defects encompass three primary classifications: gastroschisis, omphalocele and anomalies resembling body stalk. Potential causative factors include early amnion rupture, amniotic bands, vascular disruptions or abnormal folding of the ...
Nicolae Gică   +6 more
doaj   +1 more source

Case Report: Diagnosis and Management of Body Stalk Anomaly

open access: yesJurnal Kedokteran Diponegoro
Background: Body stalk anomaly is a rare and severe malformation syndrome , occurring only 1 of 10.000 live births. The patholphysiology and trigger factor of body stalk anomaly are still unknown and characterized by : abdominal wall defects, thoracoo ...
Imelda Yunitra, Yusrawati Yusrawati
doaj   +1 more source

Amniotic Band [PDF]

open access: yesProceedings of the Royal Society of Medicine, 1935
openaire   +2 more sources

Intermembraneous polyhydramnios in a pregnancy with separated membranes

open access: yesActa Obstetricia et Gynecologica Scandinavica, 1997
Soren Krue, Kjeld Leisgaard Rasmussen
doaj   +1 more source

Prenatal diagnosis of a skeletal disorder characterized by rhizomelic shortening of limbs caused by compound heterozygous variants in the PKDCC gene: Case report and literature review

open access: yesMolecular Genetics & Genomic Medicine
Background The protein kinase domain containing cytoplasmic (PKDCC) gene (OMIM#618821) is associated with bone development. Biallelic variants in the PKDCC gene can cause rhizomelic limb shortening with dysmorphic features.
Jing Wang   +7 more
doaj   +1 more source

Amniotic Band: A Rare Presentation

open access: yesIndian Journal of Dermatology, 2015
Subhash Kashyap   +2 more
openaire   +3 more sources

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