نتایج جستجو برای: Genital anomaly

تعداد نتایج: 60230  

Journal: :iranian journal of neonatology 0
abdolghader pakniyat m.d, student research committee, emergency department, arak university of medical science, arak, iran. mohammad reza fallah kidney transplantation fellowship, assistant professor, nephrology and kidney transplant research center, urmia university of medical sciences, urmia, iran zahra fakour neonatology fellowship, assistant professor, department of pediatrics, urmia university of medical sciences, urmia, iran farzad moloudi m.d, urmia university of medical sciences, urmia, iran seyran khezri bsc of midwifery, urmia university of medical sciences, urmia, iran sima masoudi msc of epidemiology, urmia university of medical sciences, urmia, iran

background: external genital anomalies are the most common congenital disorders in male infants with unknown etiology in the majority of cases. according to recent reports, incidence rate of these anomalies is rising in different countries. this study aimed to evaluate the prevalence of external genital anomalies and possible underlying factors in male newborns. methods: this cross-sectional st...

موسوی, سید عبداله, نخشب, مریم,

Aphallia or complete absence of penis is an extremely rare genitourinary anomaly derived from a faulty development of the genital tubercle during embryonic life. It usually coexists with other congenital anomalies. This anomaly has a very significant psychosocial impact on the child and parents. We describe herewith a neonate with male genotype who presented with aphallia and multiple anomalies...

درخشان, جهانگیر,

Developmental defect of Mullerian duct is a congenital malformation characterized by anomalies in famale upper genital organs. As the anomaly is associated with obstruction of the duct, other congenital anomalies of urinary tract specially ipsilateral ranal agenesis are common. This anomaly is often discovered in adolescent period and is usually asymptomatic until puberty. To discover this anom...

Journal: :nephro-urology monthly 0
seyed mohammadreza rabani beheshti teaching hospital, yasuj university of medical sciences, yasuj, ir iran; beheshti teaching hospital, yasuj university of medical sciences, yasuj, ir iran. tel: +98-9177411389, fax: +98-7412228211

although imperforate hymen is a rare condition, it is the most common obstructive anomaly of the female genital tract. the early diagnosis of this condition requires a high index of suspicion in newborns and in females without a history of menarche. hydronephrosis is a known but rare complication of an imperforate hymen. hereby we preset 2 cases of premenstrual adolescent with urinary retention...

2018
Tian-Tian Han Juan Chen Shu Wang Lan Zhu

RATIONALE A combination of Vaginal atresia and septate uterus as a novel genital malformation has been reported the first time. It offers a support for the bidirectional theory. PATIENT CONCERNS A 23-year-old woman presented with the inability to perform intercourse. The unprecedented variant was misdiagnosed by magnetic resonance imaging and ultrasonography as low vaginal atresia associated ...

Abdolghader Pakniyat, Farzad Moloudi Mohammad Reza Fallah, Seyran Khezri Sima Masoudi Zahra Fakour

Background: External genital anomalies are the most common congenital disorders in male infants with unknown etiology in the majority of cases. According to recent reports, incidence rate of these anomalies is rising in different countries. This study aimed to evaluate the prevalence of external genital anomalies and possible underlying factors in male newborns. Methods: This cross-sectional st...

2014
CE Okeke TI Anele CC Onyejelam

This is a report of the form of uterine anomaly involving a dual cervical canal in a side-by-side disposition with normal uterine cavity and normal vagina. It portrays a form of congenital uterine anomaly not explicable by the existing classical theory of mullerian anomalies. However, there has been a proposed reclassification of mullerian anomalies, which includes this type of anomaly under Ty...

2013
Madan Gopal Choudhary Prashant Babaji Nitin Sharma Dilip Dhamankar Gururaj Naregal Vijay Sunil Reddy

Emanuel syndrome (ES) is a rare anomaly characterized by a distinctive phenotype, consisting of characteristic facial dysmorphism, microcephaly, severe mental retardation, developmental delay, renal anomalies, congenital cardiac defects, and genital anomalies in boys. Here, we report a male neonate, with the classical features of Emanuel syndrome.

2015
Kimie NIIMI Ayaka OGUCHI Kenji NISHIO Yasushi OKANO Eiki TAKAHASHI

The following is a report on a congenital vaginal malformation, imperforate vagina, in the common marmoset (Callithrix jacchus). This anomaly was observed for the first time in an adult female in our research colony. There was no uterine and vaginal aplasia or atresia in her grossly normal genital tract. The plasma progesterone concentration suggested that the ovarian cycle had ceased. However,...

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