scholarly journals Single umbilical artery: A case report

1970 ◽  
Vol 1 (2) ◽  
pp. 59-60
Author(s):  
Neelam Pradhan ◽  
Raju Pradhan

A 38 years woman pregnant for the second time was diagnosed as having a fetus with a single umbilical artery while undergoing routine ultrasound at 5 months of pregnancy. Reports of single umbilical artery associated with chromosomal abnormality are about 30%. Luckily no abnormality was found at birth and thereafter in this baby. Key words: single umbilical artery, USG diagnosis and chromosomal abnormality   doi:10.3126/njog.v1i2.2400 N. J. Obstet. Gynaecol Vol. 1, No. 2, p. 59-60 Nov-Dec 2006

1999 ◽  
Vol 2 (1) ◽  
pp. 58-61 ◽  
Author(s):  
Mai P. Hoang ◽  
Kathleen S. Wilson ◽  
Nancy R. Schneider ◽  
Charles F. Timmons

A 22-week stillborn fetus with 47,XXX karyotype had lower mesodermal defects consisting of irregular fusion of the sacral vertebrae, anal agenesis, multicystic dysplasia of a horseshoe kidney, a single umbilical artery, dysplastic ovaries, and uterine hypoplasia. This case provides additional evidence for an association between trisomy X and genitourinary defects including lower mesodermal defects sequence.


2021 ◽  
Vol 6 (4) ◽  
pp. 322-324
Author(s):  
Priyatharsini Pari ◽  
Bharathi U ◽  
Pradha Velu ◽  
Sowndaravel S

Single umbilical artery (SUA) is a condition where one umbilical artery exists. Normally, the umbilical artery contains two umbilical artery and one umbilical vein. The incidence of SUA varies from 0.2% to 0.8%. We present a case of SUA in a term baby with birth weight of 1.7kg delivered by a 28-year-old mother. SUA is a condition which must be kept in mind during histopathological examination since it helps in improving the neonatal and maternal care.


2019 ◽  
Vol 8 (6) ◽  
pp. 2151
Author(s):  
IbrahimA Abdelazim ◽  
Mohannad Abu-Faza ◽  
MohamedE. S. Hamed ◽  
OsamaO Amer ◽  
Svetlana Shikanova ◽  
...  

Author(s):  
CHAITHRA KALKUR ◽  
NILOFER HALIM ◽  
ANUSHA RANGARE ◽  
Rumisha .

Ectodermal dysplasia is a heterogeneous group of inherited disorder affecting two or more ectodermally derived tissues such as skin, hair, nails, eccrine glands and teeth. The disorder is of two types: Hypohydrotic ectodermal dysplasia/Christ seimens –Touraine syndrome and Hydrotic ectodermal dysplasia/clousten syndrome. Commonly associated signs include hypohidrosis, anomalous dentition, onychodysplasia, hypotrichosis. Multidisciplinary approaches are required for optimal treatment3. Here, we present two cases of 19 and 13 year old male siblings who were diagnosed with the disorder based upon their clinical features. Key Words: ectodermal dysplasia, hypodontia; anomalous dentition.


2016 ◽  
pp. 106-109
Author(s):  
Hoang Minh Thi Nguyen ◽  
Huu Tri Nguyen ◽  
Thanh Thao Nguyen

Obturator hernia is a rare pelvic hernia which accounts for 1% of all abdominal hernia. Clinical manifestation is ussually unspecific. Obturator hernia is often diagnosed by computed tomography or ultrasound. We present a case of obturator hernia in an elderly women who was successfully diagnosed and treated at Hue Univeristy of Medicine and Pharmacy. Key words: obturator hernia, mechanical obstruction, intestinal obstruction, Richter obturator hernia, strangulation


1970 ◽  
Vol 10 (2) ◽  
pp. 133-136 ◽  
Author(s):  
NB Nagaveni ◽  
NB Radhika ◽  
KV Umashankara ◽  
TS Satisha

Transmigration of mandibular canine is an unusual phenomenon characterized by movement of the impacted canine crossing the mandibular midline. Mandibular canine are rarely found impacted in a horizontal position in the mandible. Most of the time, this entity occurred as an isolated finding. However there are reports showing association of dentigerous cyst and a hyperdontia. The purpose of this report is to present a case of transmigrated canine associated with agenesis of mandibular both central incisors which is not reported previously. Key words: Intra-osseous migration; mandibular canine; agenesis; central incisors. DOI: http://dx.doi.org/10.3329/bjms.v10i2.7810 Bangladesh Journal of Medical Science Vol.10 No.2 Apr’11 pp.133-136


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