Two Consecutive Stillbirths with Multiple Intestinal Atresias in a 30-Year-Old Female
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作者:
Mahjoub, Fatemeh
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Univ Tehran Med Sci, Pediat Ctr Excellence, Childrens Med Ctr, Dept Pathol, Tehran, IranUniv Tehran Med Sci, Pediat Ctr Excellence, Childrens Med Ctr, Dept Pathol, Tehran, Iran
Mahjoub, Fatemeh
[1
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Kadivar, Maliheh
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Univ Tehran Med Sci, Pediat Ctr Excellence, Childrens Med Ctr, Dept Pediat, Tehran, IranUniv Tehran Med Sci, Pediat Ctr Excellence, Childrens Med Ctr, Dept Pathol, Tehran, Iran
Kadivar, Maliheh
[2
]
Moradi, Behnaz
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Univ Tehran Med Sci, Sch Med, Tehran, IranUniv Tehran Med Sci, Pediat Ctr Excellence, Childrens Med Ctr, Dept Pathol, Tehran, Iran
Moradi, Behnaz
[3
]
Tabarzan, Nargess
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Univ Tehran Med Sci, Sch Med, Tehran, IranUniv Tehran Med Sci, Pediat Ctr Excellence, Childrens Med Ctr, Dept Pathol, Tehran, Iran
Tabarzan, Nargess
[3
]
机构:
[1] Univ Tehran Med Sci, Pediat Ctr Excellence, Childrens Med Ctr, Dept Pathol, Tehran, Iran
[2] Univ Tehran Med Sci, Pediat Ctr Excellence, Childrens Med Ctr, Dept Pediat, Tehran, Iran
Background: Multiple duodenal and jejuno-ileal atresias are extremely uncommon. The familial occurrence of multiple intestinal atresias is even more unusual. Also fetal death with isolated intestinal atresia very rare, and the combination of recurrent familial intestinal atresias and intra-uterine fetal death has not been reported previously. Case Presentation: We report on two cases of intra-uterine fetal death in a 30-year-old woman who is consanguineous with her husband and they have only one boy who carries chromosomal abnormality. To best of our knowledge this is the first reported case of two consecutive pregnancies with multiple intestinal atresias leading to intrauterine fetal death. Conclusion: Multiple and recurrent intestinal atresias are extremely uncommon. These rare cases may contribute to genetic mapping for intestinal atresias.
机构:
Shenzhen Univ, Affiliated Hosp 1, Dept Neurosurg, Shenzhen, Guangdong, Peoples R ChinaShenzhen Univ, Affiliated Hosp 1, Dept Neurosurg, Shenzhen, Guangdong, Peoples R China
Zhang Xie-jun
Huang Guo-dong
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Shenzhen Univ, Affiliated Hosp 1, Dept Neurosurg, Shenzhen, Guangdong, Peoples R ChinaShenzhen Univ, Affiliated Hosp 1, Dept Neurosurg, Shenzhen, Guangdong, Peoples R China
Huang Guo-dong
Ji Tao
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Shenzhen Univ, Affiliated Hosp 1, Dept Neurosurg, Shenzhen, Guangdong, Peoples R ChinaShenzhen Univ, Affiliated Hosp 1, Dept Neurosurg, Shenzhen, Guangdong, Peoples R China
Ji Tao
Zhang Xiao-biao
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Fu Dan Univ, Zhongshan Hosp, Dept Neurosurg, Shanghai, Peoples R ChinaShenzhen Univ, Affiliated Hosp 1, Dept Neurosurg, Shenzhen, Guangdong, Peoples R China
Zhang Xiao-biao
Liu Wen-lan
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Shenzhen Univ, Affiliated Hosp 1, Shenzhen Peoples Hosp 2, Cent Lab, Shenzhen, Guangdong, Peoples R ChinaShenzhen Univ, Affiliated Hosp 1, Dept Neurosurg, Shenzhen, Guangdong, Peoples R China
Liu Wen-lan
Li Wei-ping
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Shenzhen Univ, Affiliated Hosp 1, Dept Neurosurg, Shenzhen, Guangdong, Peoples R ChinaShenzhen Univ, Affiliated Hosp 1, Dept Neurosurg, Shenzhen, Guangdong, Peoples R China
机构:
Department of Paediatric Surgery, Faculty of Medicine, Al-Arab Medical University, Benghazi
Mangal Co-Op Hsg Society, Thane 400604, Maharashtra, Wagle Estate P.O.Department of Paediatric Surgery, Faculty of Medicine, Al-Arab Medical University, Benghazi
Gahukamble D.B.
Gahukamble L.D.
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Department of Pathology, Faculty of Medicine, Al-Arab Medical University, BenghaziDepartment of Paediatric Surgery, Faculty of Medicine, Al-Arab Medical University, Benghazi