The DOI matches its Crossref record; 77 of the 77 references it cites were found in a registry or an index.
Holoprosencephaly
Open accessAbstract
Holoprosencephaly (HPE) is a complex brain malformation resulting from incomplete cleavage of the prosencephalon, occurring between the 18th and the 28th day of gestation and affecting both the forebrain and the face. It is estimated to occur in 1/16,000 live births and 1/250 conceptuses. Three ranges of increasing severity are described: lobar, semi-lobar and alobar HPE. Another milder subtype of HPE called middle interhemispheric variant (MIHF) or syntelencephaly is also reported. In most of the cases, facial anomalies are observed in HPE, like cyclopia, proboscis, median or bilateral cleft lip/palate in severe forms, ocular hypotelorism or solitary median maxillary central incisor in minor forms. These latter midline defects can occur without the cerebral malformations and then are called microforms. Children with HPE have many medical problems: developmental delay and feeding difficulties, epilepsy, instability of temperature, heart rate and respiration. Endocrine disorders like diabetes insipidus, adrenal hypoplasia, hypogonadism, thyroid hypoplasia and growth hormone deficiency are frequent. To date, seven genes have been positively implicated in HPE: Sonic hedgehog (SHH), ZIC2, SIX3, TGIF, PTCH, GLI2 and TDGF1. A molecular diagnosis can be performed by gene sequencing and allele quantification for the four main genes SHH, ZIC2, SIX3 and TGIF. Major rearrangements of the subtelomeres can also be identified by multiplex ligation-dependent probe amplification (MLPA). Nevertheless, in about 70% of cases, the molecular basis of the disease remains unknown, suggesting the existence of several other candidate genes or environmental factors. Consequently, a "multiple-hit hypothesis" of genetic and/or environmental factors (like maternal diabetes) has been proposed to account for the extreme clinical variability. In a practical approach, prenatal diagnosis is based on ultrasound and magnetic resonance imaging (MRI) rather than on molecular diagnosis. Treatment is symptomatic and supportive, and requires a multidisciplinary management. Child outcome depends on the HPE severity and the medical and neurological complications associated. Severely affected children have a very poor prognosis. Mildly affected children may exhibit few symptoms and may live a normal life.
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Cites
Dickkopf-1 is a member of a new family of secreted proteins and functions in head induction
Glinka, A., Wu, W., Delius, H., Monaghan, A. P., Blumenstock, C., & Niehrs, C. (1998) · Nature · doi:10.1038/34848 · Cited by 1,608
McMahon, J. A., Takada, S., Zimmerman, L. B., Fan, C.-M., Harland, R. M., & McMahon, A. P. (1998) · Genes & Development · doi:10.1101/gad.12.10.1438 · Cited by 844
Vertebrate Hedgehog signalling modulated by induction of a Hedgehog-binding protein
Chuang, P.-T., & McMahon, A. P. (1999) · Nature · doi:10.1038/17611 · Cited by 795
DeMyer, W., Zeman, W., & Palmer, C. G. (1964) · Pediatrics · doi:10.1542/peds.34.2.256 · Cited by 683
Zebrafish organizer development and germ-layer formation require nodal-related signals
Feldman, B., Gates, M. A., Egan, E. S., Dougan, S. T., Rennebeck, G., Sirotkin, H. I., Schier, A. F., & Talbot, W. S. (1998) · Nature · doi:10.1038/26013 · Cited by 663
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly
Belloni, E., Muenke, M., Roessler, E., Traverse, G., Siegel-Bartelt, J., Frumkin, A., Mitchell, H. F., Donis-Keller, H., Helms, C., Hing, A. V., et al. (1996) · Nature Genetics · doi:10.1038/ng1196-353 · Cited by 643
Nodal is a novel TGF-β-like gene expressed in the mouse node during gastrulation
Zhou, X., Sasaki, H., Lowe, L., Hogan, B. L. M., & Kuehn, M. R. (1993) · Nature · doi:10.1038/361543a0 · Cited by 615
Relationship between asymmetric nodal expression and the direction of embryonic turning
Collignon, J., Varlet, I., & Robertson, E. J. (1996) · Nature · doi:10.1038/381155a0 · Cited by 561
Nodal signalling in vertebrate development
Schier, A. F., & Shen, M. M. (2000) · Nature · doi:10.1038/35000126 · Cited by 515
Essential Role forSonic hedgehogduring Hair Follicle Morphogenesis
Chiang, C., Swan, R. Z., Grachtchouk, M., Bolinger, M., Litingtung, Y., Robertson, E. K., Cooper, M. K., Gaffield, W., Westphal, H., Beachy, P. A., et al. (1999) · Developmental Biology · doi:10.1006/dbio.1998.9103 · Cited by 497
Cited by
The molecular genetics of holoprosencephaly
Roessler, E., & Muenke, M. (2010) · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · doi:10.1002/ajmg.c.30236 · Cited by 255
Primary cilia in neurodevelopmental disorders
Valente, E. M., Rosti, R. O., Gibbs, E., & Gleeson, J. G. (2014) · Nature Reviews Neurology · doi:10.1038/nrneurol.2013.247 · Cited by 254
The 11–13-week scan: diagnosis and outcome of holoprosencephaly, exomphalos and megacystis
Kagan, K. O., Staboulidou, I., Syngelaki, A., Cruz, J., & Nicolaides, K. H. (2010) · Ultrasound in Obstetrics & Gynecology · doi:10.1002/uog.7646 · Cited by 108
Qu, R., Xu, G., Ding, C., Jia, W., & Sun, M. (2020) · IEEE Access · doi:10.1109/access.2020.2991845 · Cited by 59
Williams syndrome transcription factor is critical for neural crest cell function in Xenopus laevis
Barnett, C., Yazgan, O., Kuo, H.-C., Malakar, S., Thomas, T., Fitzgerald, A., Harbour, W., Henry, J. J., & Krebs, J. E. (2012) · Mechanisms of Development · doi:10.1016/j.mod.2012.06.001 · Cited by 48
Metadata
- Authors
- Dubourg, C., Bendavid, C., Pasquier, L., Henry, C., Odent, S., & David, V.
- Venue
- Orphanet Journal of Rare Diseases
- Published
- 2007-02-02
- Volume
- 2
- Issue
- 1
- Pages
- 8-8
- ISSN
- 1750-1172 (ISSN-L)
- OpenAlex
- W2269171550
- Cited by
- 351
- References
- 77
- FWCI
- 22.49
- Type
- journal article
- Language
- en
- Open access
- gold
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