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Select item 105098601.

Holoprosencephaly (HPE) : case report and review of the literature

Watik Fedoua, Harrad Mouna, Said Hasana, Houssine Boufettal, Sakher Mahdaoui, Naima Samouh

Int J Surg Case Rep. 2023 Sep; 110: 108723. Published online 2023 Aug 26. doi: 10.1016/j.ijscr.2023.108723

PMCID:: PMC10509860

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Select item 103366302.

Congenital complete arhinia with alobar holoprosencephaly

Adwoa P Boakye-Yiadom, Samuel B Nguah, Haruna Mahama, Gyikua Plange-Rhule

Ghana Med J. 2022 Sep; 56(3): 231–235. doi: 10.4314/gmj.v56i3.14

PMCID:: PMC10336630

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Select item 102308313.

Semilobar Holoprosencephaly Caused by a Novel and De Novo ZIC2 Pathogenic Variant

D Nonkulovski, A Sofijanova, T Spasovska, Milanovski Gorjan, Lj Muaremoska-Kanzoska, T Arsov

Balkan J Med Genet. 2023 May; 25(2): 71–76. Published online 2023 May 2. doi: 10.2478/bjmg-2022-0017

PMCID:: PMC10230831

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Select item 101783494.

Holoprosencephaly with a Special Form of Anophthalmia Result from Experimental Induction of bmp4, Oversaturating BMP Antagonists in Zebrafish

Johannes Bulk, Valentyn Kyrychenko, Philipp M. Rensinghoff, Zahra Ghaderi Ardekani, Stephan Heermann

Int J Mol Sci. 2023 May; 24(9): 8052. Published online 2023 Apr 29. doi: 10.3390/ijms24098052

PMCID:: PMC10178349

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Select item 101371175.

Holoprosencephaly: Review of Embryology, Clinical Phenotypes, Etiology and Management

Maísa Malta, Rowim AlMutiri, Christine Saint Martin, Myriam Srour

Children (Basel) 2023 Apr; 10(4): 647. Published online 2023 Mar 30. doi: 10.3390/children10040647

PMCID:: PMC10137117

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Select item 100139916.

Holoprosencephaly in Patau Syndrome

Amanda de Souza Schlosser, Giovani José Coury Costa, Henrique Salmazo da Silva, Juan Luca Menezes de Mello, Lucy de Oliveira Gomes, Marina Michalski Oliveira Onoyama, Tatiana Martins Coury Costa

Rev Paul Pediatr. 2023; 41: e2022027. Published online 2023 Mar 13. doi: 10.1590/1984-0462/2023/41/2022027

PMCID:: PMC10013991

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Select item 99856987.

Fetal Cyclopia, Proboscis, Holoprosencephaly, and Polydactyly: A Case Report With Review of Literature

Raja Kollu, Sai Kotamraju, Seema Uligada, Mary Varunya

Cureus. 2023 Feb; 15(2): e34576. Published online 2023 Feb 2. doi: 10.7759/cureus.34576

PMCID:: PMC9985698

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Select item 99498318.

Rare manifestations of alobar holoprosencephaly and the potential causes: a report of two cases

Wael Nakawa, Sandy Alkhalil, Nafiza Martini, Ieman Alawad

Ann Med Surg (Lond) 2023 Feb; 85(2): 252–256. Published online 2023 Feb 7. doi: 10.1097/MS9.0000000000000176

PMCID:: PMC9949831

Article PubReader PDF–502K Cite

Select item 99401629.

Antenatal and Postnatal Diagnosis of Semilobar Holoprosencephaly: Two Case Reports

Benmoussa Meryem, Naggar Amine, Oukili Houssein, El Haddad Siham, Allali Nazik, Chat Latifa

Glob Pediatr Health. 2023; 10: 2333794X231156037. Published online 2023 Feb 17. doi: 10.1177/2333794X231156037

PMCID:: PMC9940162

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Select item 975750610.

Carbamazepine-Responsive Chorea in a Toddler with Semilobar Holoprosencephaly: Case Report

Leonardo Ajuz do Prado Oliveira, Izabela Mara Martins Silveira, Thiago Ribeiro e Silva, Daniel Almeida do Valle

J Pediatr Neurosci. 2021 Oct-Dec; 16(4): 335–337. Published online 2022 Jan 7. doi: 10.4103/jpn.JPN_229_20

PMCID:: PMC9757506

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Select item 943386211.

A plunging ranula in a child with holoprosencephaly: a case of unique pathophysiology and difficult airway management

Takuma Watanabe, Atsushi Yokoyama, Satoshi Shimizu, Kazuhisa Bessho

J Korean Assoc Oral Maxillofac Surg. 2022 Aug 31; 48(4): 232–236. Published online 2022 Aug 31. doi: 10.5125/jkaoms.2022.48.4.232

PMCID:: PMC9433862

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Select item 941863612.

Antenatal Ultrasonographic Diagnosis of a Constellation of Alobar Holoprosencephaly, Ethmocephaly, and Hydronephrosis in a Case of Early-Onset Intrauterine Growth Retardation: A Case Report

Prasanthi R Ghanta, Suresh Phatak, Pratik J Bhansali, Bhavik S Unadkat, Nidhi Goyal

Cureus. 2022 Jul; 14(7): e27375. Published online 2022 Jul 27. doi: 10.7759/cureus.27375

PMCID:: PMC9418636

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Select item 928883813.

Identifying environmental risk factors and gene-environment interactions in holoprosencephaly

Yonit A. Addissie, Angela Troia, Zoe C. Wong, Joshua L. Everson, Beth A. Kozel, Maximilian Muenke, Robert J. Lipinski, Kristen M.C. Malecki, Paul Kruszka

Birth Defects Res. Author manuscript; available in PMC 2022 Jul 17.

Published in final edited form as: Birth Defects Res. 2021 Jan 1; 113(1): 63–76. Published online 2020 Oct 28. doi: 10.1002/bdr2.1834

PMCID:: PMC9288838

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Select item 896804914.

Alobar holoprosencephaly with cebocephaly in a neonate: A rare case report from Northern Tanzania

Ibukun John Ariyo, Deborah N. Mchaile, Marco Magwizi, Michael Kayuza, Phillip Mrindoko, Desderius Celestine Chussi

Int J Surg Case Rep. 2022 Apr; 93: 106960. Published online 2022 Mar 28. doi: 10.1016/j.ijscr.2022.106960

PMCID:: PMC8968049

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Select item 896174915.

Mutations in phospholipase C eta-1 (PLCH1) are associated with holoprosencephaly

Ichrak Drissi, Emily Fletcher, Ranad Shaheen, Michael Nahorski, Amal M Alhashem, Steve Lisgo, Alberto Fernández-Jaén, Katherine Schon, Kalthoum Tlili-Graiess, Sarah F Smithson, Susan Lindsay, Hayley J Sharpe, Fowzan S Alkuraya, Geoff Woods

J Med Genet. 2022 Apr; 59(4): 358–365. Published online 2021 Apr 5. doi: 10.1136/jmedgenet-2020-107237