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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
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1981 1
1985 1
1987 2
1988 3
1990 2
1991 2
1992 2
1994 2
1995 1
1996 3
1997 3
1998 2
1999 2
2000 2
2001 7
2002 4
2003 2
2004 3
2005 6
2006 3
2007 7
2008 6
2009 3
2010 5
2011 6
2012 3
2014 5
2015 5
2016 1
2017 3
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2019 5
2020 6
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2022 4
2024 0

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106 results

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Quoted phrase not found in phrase index: "Holoprosencephaly 3"
Page 1
Pituitary Transcription Factor Mutations Leading to Hypopituitarism.
Gergics P. Gergics P. Exp Suppl. 2019;111:263-298. doi: 10.1007/978-3-030-25905-1_13. Exp Suppl. 2019. PMID: 31588536 Review.
It is part of a spectrum of disorders including craniofacial midline developmental defects ranging from holoprosencephaly through septo-optic dysplasia to combined and isolated pituitary hormone deficiency. ...Genetic testing in hypopituitarism is of high importance to the …
It is part of a spectrum of disorders including craniofacial midline developmental defects ranging from holoprosencephaly through sep …
Prenatal ultrasound-assisted identification of multiple malformations caused by a deletion in the long-arm end of chromosome 7 and review of the literature.
Zhao X, Sun W, Jia JA, Wei Z, Li X, Liao W, Wu J, Wang Y, Tian R. Zhao X, et al. J Matern Fetal Neonatal Med. 2022 Nov;35(22):4268-4272. doi: 10.1080/14767058.2020.1849104. Epub 2020 Nov 19. J Matern Fetal Neonatal Med. 2022. PMID: 33213225 Review.
Generally, 7q terminal deletion syndrome results in complex clinical phenotypes, such as microcephaly, growth and development retardation, holoprosencephaly, and sacral hypoplasia. Herein, we report the genetic and clinical features of a fetus with multiple malformations …
Generally, 7q terminal deletion syndrome results in complex clinical phenotypes, such as microcephaly, growth and development retardation, …
Myelomeningocele before birth.
Osaka K, Tanimura T, Hirayama A, Matsumoto S. Osaka K, et al. J Neurosurg. 1978 Nov;49(5):711-24. doi: 10.3171/jns.1978.49.5.0711. J Neurosurg. 1978. PMID: 712393
The characteristics of embryonic myeloschisis compared with spina bifida cystica in infants are: 1) the lesion is often more diffuse, involving the whole spinal cord (12 embryos); 2) the cervical cord is frequently affected (23 of the remaining 80 embryos); 3) holoprose …
The characteristics of embryonic myeloschisis compared with spina bifida cystica in infants are: 1) the lesion is often more diffuse, involv …
Prenatal exposure to pesticides and risk for holoprosencephaly: a case-control study.
Addissie YA, Kruszka P, Troia A, Wong ZC, Everson JL, Kozel BA, Lipinski RJ, Malecki KMC, Muenke M. Addissie YA, et al. Environ Health. 2020 Jun 8;19(1):65. doi: 10.1186/s12940-020-00611-z. Environ Health. 2020. PMID: 32513280 Free PMC article.
Early experimental evidence suggests an association between active ingredients in pesticides and holoprosencephaly (HPE), the most common malformation of the forebrain in humans (1 in 250 embryos). ...No associations were found for occupational exposures to pesticides duri …
Early experimental evidence suggests an association between active ingredients in pesticides and holoprosencephaly (HPE), the most co …
Development of the facial midline.
Carstens MH. Carstens MH. J Craniofac Surg. 2002 Jan;13(1):129-87; discussion 188-90. doi: 10.1097/00001665-200201000-00032. J Craniofac Surg. 2002. PMID: 11887012 Review.
"Intellectual excellence lies in having faith in the observation of apparently nontranscendental and unimportant facts. To observe an anatomic element calmly, with an open, analytical spirit, and with spiritual freedom, can lead to an explosive vortex of new knowled …
"Intellectual excellence lies in having faith in the observation of apparently nontranscendental and unimportant facts. To observe …
Risk of Stillbirth for Fetuses With Specific Birth Defects.
Heinke D, Nestoridi E, Hernandez-Diaz S, Williams PL, Rich-Edwards JW, Lin AE, Van Bennekom CM, Mitchell AA, Nembhard WN, Fretts RC, Roberts DJ, Duke CW, Carmichael SL, Yazdy MM; National Birth Defects Prevention Study. Heinke D, et al. Obstet Gynecol. 2020 Jan;135(1):133-140. doi: 10.1097/AOG.0000000000003614. Obstet Gynecol. 2020. PMID: 31809437 Free PMC article.
Among those with isolated birth defects not affecting major vital organs, elevated risks (per 1,000 fetuses) were observed for cleft lip with cleft palate (10; 95% CI 7-15), transverse limb deficiencies (26; 95% CI 16-39), longitudinal limb deficiencies (11; 95% CI 3 …
Among those with isolated birth defects not affecting major vital organs, elevated risks (per 1,000 fetuses) were observed for cleft …
The spectrum of orofacial clefting.
Eppley BL, van Aalst JA, Robey A, Havlik RJ, Sadove AM. Eppley BL, et al. Plast Reconstr Surg. 2005 Jun;115(7):101e-114e. doi: 10.1097/01.prs.0000164494.45986.91. Plast Reconstr Surg. 2005. PMID: 15923821 Review.
Define the sites of anatomical disruption and deformities that these types of facial clefts cause. 3. Describe the cause and incidence, if known, of orofacial clefts and their inheritance/transmission risks. ...However, atypical forms of clefts with lip involvement also oc …
Define the sites of anatomical disruption and deformities that these types of facial clefts cause. 3. Describe the cause and incidenc …
Alobar holoprosencephaly associated with a rare chromosomal abnormality: Case report and literature review.
Ionescu CA, Calin D, Navolan D, Matei A, Dimitriu M, Herghelegiu C, Ples L. Ionescu CA, et al. Medicine (Baltimore). 2018 Jul;97(29):e11521. doi: 10.1097/MD.0000000000011521. Medicine (Baltimore). 2018. PMID: 30024536 Free PMC article. Review.
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 t …
INTERVENTIONS: A cesarean section at 38 weeks was indicated for fetal bradycardia and a female baby was delivered, with Apgar score 6 …
Human prenatal craniofacial development related to brain development under normal and pathologic conditions.
Kjaer I. Kjaer I. Acta Odontol Scand. 1995 Jun;53(3):135-43. doi: 10.3109/00016359509005963. Acta Odontol Scand. 1995. PMID: 7572088 Review.
Then, developmental interrelationships are illustrated under normal and pathologic conditions (cleft lip and palate, holoprosencephaly, anencephaly, amniotic band sequence). New observations are described in detail, and references are given to previously published a …
Then, developmental interrelationships are illustrated under normal and pathologic conditions (cleft lip and palate, holoprosencephaly …
Prenatal sonographic features of fetuses in trisomy 13 pregnancies (I).
Chen CP. Chen CP. Taiwan J Obstet Gynecol. 2009 Sep;48(3):210-7. doi: 10.1016/S1028-4559(09)60292-8. Taiwan J Obstet Gynecol. 2009. PMID: 19797008 Free article. Review.
This article provides a comprehensive review of the prenatal sonographic features of trisomy 13, including the major structural abnormalities observed during the first trimester (omphalocele, holoprosencephaly, megacystis and congenital heart defects), the frequenci …
This article provides a comprehensive review of the prenatal sonographic features of trisomy 13, including the major structural abnormalitie …
106 results