Alobar holoprosencephaly associated with a rare chromosomal abnormality: Case report and literature review
| Autor: | Cringu Antoniu Ionescu, Mihai Dimitriu, Liana Ples, Alexandra Matei, C. Herghelegiu, Dan Navolan, Dan Calin |
|---|---|
| Rok vydání: | 2018 |
| Předmět: |
0301 basic medicine
hypotelorism Pathology medicine.medical_specialty Karyotype Chromosome Disorders Gestational Age Ultrasonography Prenatal 03 medical and health sciences Craniosynostoses 0302 clinical medicine Holoprosencephaly Pregnancy Chromosomal Abnormality facial abnormalities Medicine Humans Abnormalities Multiple Clinical Case Report microcephaly single nostril nose 030219 obstetrics & reproductive medicine business.industry Mosaicism Infant Newborn Gestational age Brain General Medicine medicine.disease Delivery Obstetric Alobar holoprosencephaly Magnetic Resonance Imaging cebocephaly 030104 developmental biology nervous system Forebrain Cebocephaly Female business Chromosomes Human Pair 18 Research Article |
| Zdroj: | Medicine |
| ISSN: | 1536-5964 |
| Popis: | Rationale: Holoprosencephaly is a structural malformation of the brain that results from the complete or incomplete noncleavage of the forebrain of the embryo into 2 hemispheres. We report a severe case of alobar holoprosencephaly diagnosed at 38 weeks, associated with cebocephaly, microcephaly, and craniosynostosis. Patient concern: The main knowledge added by this case is the late ultrasound diagnosis and chromosomal analysis that revealed a very rare abnormality (45X/46,XX/47,XX) with mosaicism at chromosome 18. Diagnoses: Investigation of the mother revealed nothing remarkable from clinical point of view and on laboratory tests. Ultrasonography identified a fetal biometry appropriate for gestational age, except for the head biometry and abdominal circumference, that were appropriate for less than the fifth percentile. Microcephaly, a large midline monoventricle, absent midlinestructures, cleft lip, cebocephaly (hypotelorism, single-nostril nose), ethmocephaly (hypotelorism, interorbital proboscis) and craniosynostosis, were also present. Fetal magnetic resonance imaging of fetus revealed an absent midline structure, a central monoventricle, abnormal corpus calosum, and abnormal gyri. Interventions: A cesarean section at 38 weeks was indicated for fetal bradycardia and a female baby was delivered, with Apgar score 6, weight 2290g. After birth, the diagnosis of the fetus confirmed holoprosencephaly with facial anomalies and demonstrated repeated tonic-clonic seizure, severe respiratory failure, cyanosis, decreased muscle tone, palor, and apnea. Laboratory examination of the newborn revealed acidosis and a prolonged of prothrombin time. The neonate was treated for severe respiratory distress syndrome, with immediate intubation and resuscitation. Vitamin K, fresh frozen plasma, and antibiotics were also administered. Outcomes: After delivery, exitus of the fetus occurred at 3 days and 18hours due to massive pulmonary hemorrhage. Lessons: We described a case of alobar holoprosencephaly diagnosed at 38 weeks of gestation and associated with a rare chromosomal abnormality (45X/46,XX/47,XX) with mosaicism at chromosome 18. Emotional implications could have been less severe if the patient underwent regular ultrasonography allowing a diagnosis in the first or early second trimester. |
| Databáze: | OpenAIRE |
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