Left Nostril Agenesis in a Fetus with VACTERL Association: A Case Report

نویسندگان

چکیده

VACTERL association represents a rare condition with broad spectrum of coexisting congenital abnormalities. Although multifactorial origin has been described, the etiology is still unclear. Prenatal diagnosis can be challenging, as specific characteristics may difficult to determined before birth. This case report describes finding multiple abnormalities in male fetus at 30 weeks gestation. The most notable findings were presence duodenal stenosis, esophageal atresia distal tracheoesophageal fistula (type 3), interatrial septal communication foramen ovale, and left nostril choana agenesis. After birth making differential diagnosis, all these oriented towards association. To best our knowledge, no cases unilateral agenesis have previously described.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Case Report: VACTERL association

VACTERL association is a useful acronym for a condition characterised by the sporadic, non-random association of specific birth defects of multiple organ systems.We present one such case which had congenital abnormalities of renal,skeletal and cardiac system.

متن کامل

Association of Nasal Nostril Stenosis with Bilateral Choanal Atresia: A Case Report

Introduction: Neonatal nasal airway obstruction induces various degrees of respiratory distress. The management of this disease, including surgical repair, will depend on the severity and location of the obstruction. We describe here a case of congenital nasal nostril stenosis that required surgical repair for stenting of both nares after coanal atresia repair.   Case Report: A 2 days old femal...

متن کامل

A Case Report of Penis Agenesis (Aphallia)

A neonate was admitted on the second day of birth in the pediatric ward of Kerman medical sciences university No. 1 Hospital, because of abdominal distention and the absence of penis. Physical findings were lethargia, infancy hyporeflexia, abdominal distention without any organomegally, absence of penis, two touchable masses in the scrotum and a hole on scrotum for urine discharge. CBC and e...

متن کامل

Placental Mesenchymal Dysplasia With Normal Fetus: A Rare Case Report

Placental mesenchymal dysplasia (PMD) is a rare benign placental abnormality. It is characterized by hydropic degeneration of stem villi, placentomegaly, and increased maternal serum alpha-fetoprotein(AFP). It can be associated with different congenital abnormalities, karyotype abnormalities, and feto-maternal morbidities. It is difficult to differentiate PMDfrom partial mole, complete mole wit...

متن کامل

Birth of a live fetus in twin pregnancy with hydatidiform mole and co-existent a live fetus: case report

Background: Twin pregnancy consist a healthy fetus, and hydatidium molar pregnancy is unusual and very rare. Its incidence is in about 1,22,000 to 1,100,000 of all pregnancies. This type of pregnancy is commonly associated with several obstetric complications requiring early termination of pregnancy. Managing a twin mole pregnancy with normal and live fetuses is controversial, although this unu...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Open Journal of Obstetrics and Gynecology

سال: 2023

ISSN: ['2160-8806', '2160-8792']

DOI: https://doi.org/10.4236/ojog.2023.134058