Results 31 to 40 of about 31,090 (171)
Thoracopagus parasitic twin with omphalocele rupture: a case report
Background: Heteropagus or parasitic twin is a rare congenital anomaly that affects two connected children with imprecisely understood anatomy and physiology. This case report aims to describe a thoracopagus patient with severe complications. Case presentation: One-day-old female baby was born with thoracopagus and omphalocele rupture.
Made Indah Pradnya Paramita +4 more
openaire +1 more source
Tujuan: Melaporkan kasus omphalocele Metode: Laporan kasus Hasil: Kasus wanita berusia 24 tahun, dengan diagnosa G1P0A0H0 gravid aterm 37-38 minggu + omphalocele + IUGR. Pada pemeriksaan USG ditemukan biometri janin; BPD : 84 mm, FL : 67 mm ...
Yusrawati Yusrawati +1 more
core +1 more source
Chromosomal Abnormalities Associated With Omphalocele [PDF]
SummaryFetuses with omphalocele have an increased risk for chromosomal abnormalities. The risk varies with maternal age, gestational age at diagnosis, association with umbilical cord cysts, complexity of associated anomalies, and the contents of ...
Chih-Ping Chen, Chen, Chih-Ping
core +1 more source
An Epigastric Heteropagus Twin with Ruptured Giant Omphalocele
We present a case of heteropagus twins attached to the epigastric region. The neonate also had ruptured giant omphalocoele with most of gut and liver lying outside the abdominal cavity. Patient had uneventful surgery for separation of twins and repair of ruptured omphalocoele.
Sajid Hameed, Dar +4 more
openaire +3 more sources
Perinatal omphalocele rupture is a rare occurrence. We present a case of a baby delivered at 35 weeks with a known giant omphalocele, transverse lie, and the omphalocele downward in the birth canal who suffered rupture of the omphalocele and liver injury
Maria E. Linnaus +4 more
doaj +1 more source
Background Kagami–Ogata syndrome is also known as paternal uniparental disomy 14 and related disorders and is caused by abnormal genomic imprinting in the long arm of the chromosome 14q32.2 region.
Haipeng Huang +11 more
doaj +1 more source
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken +4 more
wiley +1 more source
Scientific Report on consumer health‐based guidance values for trifluoroacetic acid
Abstract The European Commission asked EFSA to provide a scientific report according to Article 31 of Regulation (EC) No 178/2002, in conjunction with Regulation (EC) No 1107/2009, to revise consumer health‐based guidance values, i.e. acceptable daily intake (ADI) and acute reference dose (ARfD), for trifluoroacetic acid (TFA). EFSA launched a targeted
EFSA (European Food Safety Authority) +15 more
wiley +1 more source
Diverse mechanisms underlying the fetal growth course in gastroschisis and omphalocele [PDF]
BACKGROUND Gastroschisis and omphalocele are the 2 most common congenital fetal abdominal wall defects. Both malformations are commonly associated with small-for-gestational-age neonates.
Amylidi-Mohr, Sofia +9 more
core +2 more sources
Formal saline versus honey as escharotic in the conservative management of major omphaloceles
Background: The use of honey as an escharotic agent in the conservative management of omphalocele major has not been widely explored in spite of its proven benefits in chronic wound management. We explored the use of local honey as an escharotic agent by
Christopher O Bode +2 more
doaj +1 more source

