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1.
Prenat Diagn ; 39(6): 415-419, 2019 05.
Artigo em Inglês | MEDLINE | ID: mdl-30900264

RESUMO

Solitary median maxillary central incisor (SMMCI) syndrome is a complex disorder consisting of multiple, developmental defects involving midline structures of the head, which includes the cranial bones, the maxilla, and its container dentition (specifically the central incisor tooth germ), together with other midline structures of the body. SMMCI may appear as an isolated trait or in association with other midline developmental anomalies. We describe the case of a patient with SMMCI. He presented with a solitary median maxillary incisor, short stature, corpus callosum anomalies and a microform of holoprosencephaly (HPE), diabetes insipidus, and neurodevelopmental delay. The diagnosis was performed postnatally based on clinical features, radiological imaging, and a comprehensive genetic study. SMMCI can be diagnosed during the prenatal or neonatal periods or during infancy. Evaluation of the superior maxillary bone is important for prenatal diagnosis. Direct evaluation through bidimensional ultrasound or the use of multiplanar ultrasound or tridimensional reconstruction should be performed in cases of brain or face malformations. Early diagnosis can contribute to improved prenatal assessment and postnatal management.


Assuntos
Anormalidades Múltiplas/diagnóstico , Anodontia/diagnóstico , Incisivo/anormalidades , Diagnóstico Pré-Natal , Anormalidades Múltiplas/patologia , Anodontia/complicações , Anodontia/patologia , Feminino , Holoprosencefalia/complicações , Holoprosencefalia/diagnóstico , Holoprosencefalia/patologia , Humanos , Incisivo/patologia , Lactente , Recém-Nascido , Masculino , Maxila/anormalidades , Fenótipo , Gravidez , Prognóstico , Síndrome , Adulto Jovem
2.
J Clin Ultrasound ; 46(8): 549-552, 2018 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-29570797

RESUMO

Congenital imperforate hymen is probably the most common obstructive anomaly of the female reproductive tract. The accumulation of fluid in the genital tract leads to a distended uterus and vagina, causing hydrometrocolpos. Prenatal diagnosis of fetal hydrometrocolpos is uncommon, with only 22 cases reported in the literature and only a few cases of prenatal imaging of this condition available to date. The main ultrasound finding is a fetal pelvic mass posterior to the bladder and anterior to the rectum. We present the case of a 37-week female fetus with a fetal pelvic mass detected in a routine obstetric ultrasound examination, and the correlation between the prenatal and postnatal findings.


Assuntos
Hidrocolpos/diagnóstico por imagem , Hímen/anormalidades , Distúrbios Menstruais/diagnóstico por imagem , Ultrassonografia Pré-Natal , Adulto , Anormalidades Congênitas , Feminino , Humanos , Hidrocolpos/complicações , Hidrocolpos/congênito , Hímen/diagnóstico por imagem , Recém-Nascido , Distúrbios Menstruais/complicações , Distúrbios Menstruais/congênito , Gravidez
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