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Thematische Bibliographien / Alobar holoprosencephaly

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Auswahl der wissenschaftlichen Literatur zum Thema „Alobar holoprosencephaly“

Autor: Grafiati

Veröffentlicht am 30. Juni 2021

Zuletzt aktualisiert am 29. Juli 2025

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Zeitschriftenartikel zum Thema "Alobar holoprosencephaly"

1

Riu, Deviana Soraya, and Efendi Lukas. "Tiga Kasus Holoprosensefal Alobar Dengan Variasi Gambaran Klinis : Diagnosis Ultrasonografi." Indonesian Journal of Obstetrics & Gynecology Science 5, no. 1 (2022): 150–57. http://dx.doi.org/10.24198/obgynia/v5n1.382.

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Holoprosensefal (HPE) adalah spektrum malformasi dengan berbagai hasil luaran. Laporan ini menjelaskan 3 kasus holoprosensefal alobar yang dikonfirmasi saat antenatal dengan pemeriksaan ultrasonografi (USG). Selain gambaran holoprosensefal alobar yang serupa pada ketiga kasus, ditemukan gambaran lain yaitu probosis, siklops, kelainan jantung, dan arteri umbilikalis tunggal. Gambaran klinis yang berbeda adalah preeklamsia, polidaktili, dan mikropenis pada kasus pertama, pada kasus kedua adalah mielomeningokel; dan hidransefal untuk kasus ketiga. Analisis kromosom dilakukan hanya pada kasus kedu

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2

Selden, Nathan. "Alobar Holoprosencephaly." Pediatric Neurosurgery 33, no. 2 (2000): 112. http://dx.doi.org/10.1159/000028986.

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3

Riu, Deviana Soraya, and Efendi Lukas. "Tiga Kasus Holoprosensefal Alobar dengan Variasi Gambaran Klinis:Diagnosis Ultrasonografi." Indonesian Journal of Obstetrics & Gynecology Science 5, no. 1 (2022): 150. http://dx.doi.org/10.24198/obgynia.v5i1.382.

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Holoprosensefal (HPE) adalah spektrum malformasi dengan berbagai hasil luaran. Laporan ini menjelaskan 3 kasus holoprosensefal alobar yang dikonfirmasi saat antenatal dengan pemeriksaan ultrasonografi (USG). Selain gambaran holoprosensefal alobar yang serupa pada ketiga kasus, ditemukan gambaran lain yaitu probosis, siklops, kelainan jantung, dan arteri umbilikalis tunggal. Gambaran klinis yang berbeda adalah preeklamsia, polidaktili, dan mikropenis pada kasus pertama, pada kasus kedua adalah mielomeningokel; dan hidransefal untuk kasus ketiga. Analisis kromosom dilakukan hanya pada kasus kedu

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4

Callahan, Jodi, Casey Harmon, John Aleshire, Bill Hickey, and Brandy Jones. "Alobar Holoprosencephaly With Cebocephaly." Journal of Diagnostic Medical Sonography 33, no. 1 (2016): 39–42. http://dx.doi.org/10.1177/8756479316664477.

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Holoprosencephaly (HPE) is a complex brain malformation caused by incomplete fusion of cleavage of the cerebral hemispheres and deep brain structures affecting 6 to 12:10,000 live-born infants. There are three categories of HPE ranging in severity, with alobar holoprosencephaly being the most severe, followed by semilobar holoprosencephaly, and lobar holoprosencephaly being the mildest form. Facial anomalies as well as chromosome anomalies are often associated with HPE. This case study describes a transabdominal sonographic diagnosis of alobar HPE with cebocephaly originally found at 27 weeks

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Jalal, Mohammed, Imane El Abbassi, Ayoub Amghar, Amine Lamrissi, and Said Bouhya. "Alobar holoprosencephaly: A case report." Edorium Journal of Gynecology and Obstetrics 7, no. 2 (2023): 1–4. http://dx.doi.org/10.5348/100032g06mj2023cr.

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Introduction: Holoprosencephaly (HPE) is a rare brain malformation, which results from a cleavage defect of the prosencephalon. Three forms have been described as: alobar, semi-lobar, and lobar forms. Case Report: We report a rare case of holoprosencephaly, diagnosed at the maternity of the Ibn Rochd Hospital Center in Casablanca. Conclusion: Holoprosencephaly is secondary to a cleavage anomaly of the prosencephalon, the diagnosis is based on echotomography, computed tomography (CT) scan and nuclear magnetic resonance imaging (MRI). It is important to perform a karyotype to look for a chromoso

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Karantanas, A. H., N. Papanikolaou, A. Danos, and G. Antonakopoulos. "Cyclopia and exadactyly: CT and MRI findings." Dentomaxillofacial Radiology 28, no. 6 (1999): 372–74. http://dx.doi.org/10.1038/sj/dmfr/4600469.

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Abstract Cyclopia is a congenital abnormality consisting of fused orbits and a single eye and is the most extreme form of alobar holoprosencephaly. The present case describes the CT and MRI findings in the skull of a 33-week-old cadaver with alobar holoprosencephaly and exadactyly.

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Halim, H. "Alobar Holoprosencephaly : A Case Report." Journal of Medical Science And clinical Research 11, no. 12 (2023): 13–17. http://dx.doi.org/10.18535/jmscr/v11i12.03.

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Holoprosencephaly (HPE) consists of a spectrum of malformations related to incomplete separation of the prosencephalon. It occurs between the 18th and the 28th day of gestation and affects both the forebrain and the face. It is estimated to occur in 1/16,000 live births and 1/250 conceptuses. Alobar HPE, the most common and most severe type of HPE, can be diagnosed in the first trimester of pregnancy using ultrasound. Among survivors, the long-term outcome is poor and depends on the type and severity of the pathology as well as associated anomalies. Keywords : Holoprosencephaly, Alobar, Malfor

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Sharma, Dr Bandana, HIMANI MALVIYA, Dr Anchal Malik, and Rahul Ray. "A rare occurrence: A case report on alobar holoprosencephaly with cyclopia." Indian Journal of Case Reports 10, no. 7 (2024): 205–7. http://dx.doi.org/10.32677/ijcr.v10i7.4582.

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Alobar holoprosencephaly with cyclopia is a rare lethal congenital anomaly frequently accompanied by other malformations and characterized by large variations in incidence. Alobar holoprosencephaly presents as a congenital brain malformation characterized by the incomplete separation of the brain hemispheres during fetal development, typically occurring between the 4th and 6th gestational weeks, affecting about 1 in 250 conceptuses and 1 in 16,000 live births. This anomaly involves the failure of transverse cleavage into the diencephalon and telencephalon and is often accompanied by various mi

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Nechaev, Vladimir N., and Yuri V. Chernenkov. "Alobar form of holoprosencephaly in the fetus and newborn (clinical case)." Saratov Journal of Medical Scientific Research 19, no. 3 (2023): 267–72. http://dx.doi.org/10.15275/ssmj1903267.

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Objective: on the clinical example of the alobar form of fetal and newborn holoprosencephaly, to consider the risk factors for the development of a congenital anomaly and the possibilities of a tactical solution. This clinical case focuses our attention on the complexity of early diagnosis of this congenital pathology, prevention and choosing the right solution to the problem. Differential diagnosis of the alobar form with seven-lobarand other types of holoprosencephaly was carried out. A clinical case of congenital alobar holoprosencephaly was diagnosed prenatally, with a gestation period of

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Raman, Rajesh, and Geetha Mukunda Jagadesh. "Antenatal Diagnosis of Alobar Holoprosencephaly." Case Reports in Radiology 2014 (2014): 1–4. http://dx.doi.org/10.1155/2014/724671.

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A twenty-year-old second gravida presented to the department of radiodiagnosis for routine obstetric ultrasound examination. Ultrasonography revealed a live fetus of 17 weeks with absent falx, fused thalami, monoventricle, proboscis, and cyclopia. Fetal MRI was performed and the findings were confirmed. Even though ultrasonography is diagnostic in the detection of fetal anomalies, MRI plays a vital role due to its multiplanar capability and excellent soft tissue resolution. The importance of presenting this classical case of alobar holoprosencephaly is to sensitize the clinicians and radiologi

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Dissertationen zum Thema "Alobar holoprosencephaly"

1

Elfarawi, Hunaydah. "Alobar Holoprosencephaly: Parental Perspectives on Prenatal Decision-making, Prenatal Provider Prognostication, and Quality of Life." University of Cincinnati / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1617108856885634.

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JAMOT, FOURNERON CHRISTINE. "L'holoprosencephalite alobaire et son diagnostic echographique : a propos d'un cas." Saint-Etienne, 1992. http://www.theses.fr/1992STET6221.

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Buchteile zum Thema "Alobar holoprosencephaly"

1

"Alobar Holoprosencephaly." In Diagnostic Imaging: Obstetrics. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-39256-3.50033-9.

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2

Barness, Lewis A., Enid Gilbert-Barness, and Dean Fauber. "Endocrine." In Handbook of: Pediatric Physical and Clinical Diagnosis. Oxford University PressNew York, NY, 2008. http://dx.doi.org/10.1093/oso/9780195373257.003.0016.

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Abstract Pituitary The pituitary is the master hormone responsible for the activity of many of the other hormones, including human growth hormone, which is responsible for growth. Pituitary agenesis may be familial in rare instances and may be associated with one variety of congenital hypopituitarism or with major craniofacial anomalies (e.g., alobar holoprosencephaly or facial clefts) and in anencephalics. Infants with isolated pituitary aplasia may have normal intrauterine growth but present with neonatal hypoglycemia.

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3

Malviya, Himani, Bandana Sharma, Rahul Ray, and Anchal Malik. "Alobar Holoprosencephaly with Cyclopia: An In-Depth Exploration." In Medicine and Medical Research: New Perspectives Vol. 12. BP International, 2024. http://dx.doi.org/10.9734/bpi/mmrnp/v12/2236.

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4

Domm, Christian, Paul-Martin Holterhus, and Heiner Moenig. "19-Year-Old Female with Hypodipsia-Hypernatremia-Syndrome Due to Alobar Holoprosencephaly." In The Endocrine Society's 93rd Annual Meeting & Expo, June 4–7, 2011 - Boston. The Endocrine Society, 2011. http://dx.doi.org/10.1210/endo-meetings.2011.part4.p14.p3-754.

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