[HTML][HTML] The etiopathogenic and morphological spectrum of anencephaly: a comprehensive review of literature

O Munteanu, MM Cîrstoiu, FM Filipoiu… - Romanian Journal of …, 2020 - ncbi.nlm.nih.gov
Anencephaly is a severe malformation of the central nervous system (CNS), being one of the
most common types of neural tube defects. It is defined as total or partial absence of the …

Prenatal diagnosis of craniorachischisis totalis

P Costa, AF Oliveira, AB Vilaça - BMJ Case Reports CP, 2022 - casereports.bmj.com
Craniorachischisis totalis (anencephaly with total open spina bifida) is the most severe form
of neural tube defects. The exact aetiology of neural tube defects remains poorly …

Anomalies of the Mesenchyme (Meninges and Skull)—Defects of Neural Tube Closure: Cephalocele and Other Calvarial and Skull Base Defects; Intracranial Lipomas …

S Carnazzo, D La Cognata, A Zanghì… - Journal of Pediatric …, 2024 - thieme-connect.com
Within the embryonic head, a layer of mesenchyme envelops the brain beneath the surface
ectoderm. This cranial mesenchyme is responsible for the formation of the meninges, the …

[HTML][HTML] Sirenomelia-A rare congenital anomaly: Case report

D Thombare, P Dixit, A Chavan… - Journal of Education and …, 2023 - journals.lww.com
Sirenomelia is an extremely uncommon congenital deformity in which neonate has fused
lower limbs associated with various visceral malformations including urogenital and …

Prenatal sonographic image of sirenomelia with anencephaly and craniorachischisis totalis

T Sugiura, Y Sato, N Nakanami… - Case Reports in …, 2018 - Wiley Online Library
Sirenomelia is a rare congenital malformation characterized by varying degrees of fusion of
the lower extremities. It is commonly associated with severe urogenital and gastrointestinal …

[HTML][HTML] Sirenomelia: A case report

P Kattel - JNMA: Journal of the Nepal Medical Association, 2018 - ncbi.nlm.nih.gov
Sirenomelia is primarily a congenital anomaly where a normally paired lower limb is
replaced by a single midline limb and is characterized by single umbilical artery. Such cases …

Sirenomelia: a rare case report from rural hospital of Nepal

S Shrestha, KP Thani, M Keshari, A Shrestha… - Journal of Chitwan …, 2022 - jcmc.com.np
Sirenomelia (mermaid syndrome) is a rare congenital fetal anomaly with characteristic
feature of complete or partial fusion of lower limbs. Additional malformations are …

[PDF][PDF] LİTERATÜR EŞLİĞİNDE 36 FETAL OTOPSİ SONUÇLARININ DEĞERLENDİRİLMESİ: RETROSPEKTİF KLİNİK ÇALIŞMA Assessment of 36 Fetal Autopsy …

CC Goret - Bozok Tıp Dergisi - dergipark.org.tr
ÖZETAmaç: Perinatal otopsi, termine edilmiş/abort ile sonlanmış fetüslerin veya ölen
yenidoğan/infantların anomalilerini saptamak için hala altın standart prosedür olarak …

Sirenomelia: a case report.

PK Pramod Kattel - 2018 - cabidigitallibrary.org
Sirenomelia is primarily a congenital anomaly where a normally paired lower limb is
replaced by a single midline limb and is characterized by single umbilical artery. Such cases …

[PDF][PDF] Case Report Prenatal Sonographic Image of Sirenomelia with Anencephaly and Craniorachischisis Totalis

T Sugiura, Y Sato, N Nakanami, K Tsukimori - 2018 - academia.edu
Sirenomelia is a rare congenital malformation characterized by varying degrees of fusion of
the lower extremities. It is commonly associated with severe urogenital and gastrointestinal …