Academic literature on the topic 'Miller-Dieker'

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Journal articles on the topic "Miller-Dieker"

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Gräfe, L., U. Schneider, C. Springer, and D. Huhle. "Miller-Dieker-Syndrom." Geburtshilfe und Frauenheilkunde 77, no. 04 (2017): 406–29. http://dx.doi.org/10.1055/s-0037-1601514.

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Alvarado, Monica. "Miller-Dieker Syndrome." American Journal of Diseases of Children 147, no. 12 (1993): 1291. http://dx.doi.org/10.1001/archpedi.1993.02160360033012.

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Mendoza Torres, José Cruz, and Nelson Ramón Coiscou Domínguez. "Síndrome de Miller-Dieker: reporte de dos casos." Revista de la Facultad de Medicina 67, no. 2 (2024): 19–25. http://dx.doi.org/10.22201/fm.24484865e.2024.67.2.03.

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Introduction: Miller-Dieker syndrome has an autosomal dominant pattern of inheritance and belongs to the group of neuronal migration disorders. It is characterized by the presence of type 1 lissencephaly, global development delay, microcephaly, epilepsy and facial dysmorphisms caused by mutations in chromosome 17p13. Miller-Dieker syndrome is an extremely rare disease with a prevalence of 1 case per 100,000 live births. Case presentation: We present two cases of Miller-Dieker syndrome in which data from the physical examination and questioning were clues that allowed a strong diagnostic suspicion and that, in turn, the definitive diagnosis by means of FISH allowed us to provide adequate management in order to improve the long-term prognosis. Conclusion: A high diagnostic suspicion must be achieved through physical examination aimed at identifying alterations in patients with difficult-to-control epilepsy, since it allows guiding the etiological diagnosis and thereby providing adequate treatment. Keywords: Miller-Dieker syndrome; lissencephaly type 1; chromosome 17p13.3 deletion syndrome; epilepsy; microcephaly
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Iglesias Escalera, G., M. L. Carrasco Marina, F. Martín del Valle, N. Martínez Guardia, L. Rodríguez, and M. L. Martínez-Fernández. "Síndrome de Miller-Dieker." Anales de Pediatría 70, no. 3 (2009): 304–6. http://dx.doi.org/10.1016/j.anpedi.2008.11.003.

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Delgado Gutiérrez, J., J. Quintero, and W. Saldarriaga. "P04.10: Miller-Dieker syndrome." Ultrasound in Obstetrics & Gynecology 44, S1 (2014): 204. http://dx.doi.org/10.1002/uog.14063.

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Lahiri, Keya, Fehmida Najmuddin, Rajesh Rai, and Priya Patil Cholera. "Miller–Dieker syndrome with hydronephrosis." International Journal of Case Reports and Images 6, no. 10 (2015): 610. http://dx.doi.org/10.5348/ijcri-201598-cr-10559.

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Bahmad, Hisham F., Lauren Ramesar, Cecilia Nosti, et al. "RETRACTED: Bahmad et al. Histopathologic Findings Associated with Miller–Dieker Syndrome: An Autopsy Report. Diseases 2022, 10, 95." Diseases 12, no. 1 (2023): 2. http://dx.doi.org/10.3390/diseases12010002.

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Pati, Sananda, Sangita De, Sankha Subhra Nag, and Kaustav Nayek. "Miller Dieker Syndrome as a Cause of Refractory Seizures." Journal of Nepal Paediatric Society 34, no. 2 (2014): 154–56. http://dx.doi.org/10.3126/jnps.v34i2.9408.

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Miller-Dieker syndrome is a genetic deletion syndrome characterized by neuronal migration disorder lissencephaly where the exterior of the brain is abnormally smooth with fewer folds and grooves and characteristic facial dysmorphism. A one year old boy born presented to our emergency with severe respiratory distress and recurrent convulsions. A diagnosis of Miller Diecker syndrome was made consistent with typical clinical features and investigations. The child was managed symptomatically, however the seizures remained refractory and the child succumbed on day three of admission. Diagnosis of rare diseases like this is necessary not only for management but also for predicting recurrence in the family and genetic counselling. Key words: Miller Dieker syndrome; Lissencephaly; Refractory Seizures DOI: http://dx.doi.org/10.3126/jnps.v34i2.9408J Nepal Paediatr Soc 2014;34(2):154-156
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Herman, T. E., and M. J. Siegel. "Miller–Dieker syndrome, type 1 lissencephaly." Journal of Perinatology 28, no. 4 (2008): 313–15. http://dx.doi.org/10.1038/sj.jp.7211920.

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Marino, S1 Falsaperla R1 Marino SD1 Smilari P2 Greco F. 2. Vitaliti G. 1. Caccamo M2 Barbagallo M3 &. *Pavone P1 2. "WEST VARIANT IN MILLER-DIEKER SYNDROME." GLOBAL JOURNAL OF ENGINEERING SCIENCE AND RESEARCHES 5, no. 9 (2018): 1–5. https://doi.org/10.5281/zenodo.1420146.

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<strong>Introduction. </strong>Miller-Dieker syndrome (MDs) is a severe malformative condition characterized by a smooth surface known also as lissencephaly . The syndrome is linked to a contiguous gene deletion of short arm of chromosome 17 (17p13.3) causing cerebral dysregulation. &nbsp;Affected children present with facial dysmorphisms, severe intellectual disability and drug resistant seizures. Infantile spasms are the most frequently reported types of seizures with the EEG recording presenting with the typical aspect of hypsarrhythmia<strong>. </strong> <strong>Case Report. </strong>Recently an infant with MDs was diagnosed soon after birth and followed up for 12 months with clinical and serial electroencephalographic (EEG) recording. &nbsp;During the course of the disorder, wide variability of the clinical and EEGraphic pattern were reported. At the age of 6 months the EEG showed a pattern of modified hypsarrhythmia&nbsp; &nbsp;without the classic clinical association with infantile spasms which recurred afterward. <strong>Conclusion.</strong> We have hypothesized the EEG&nbsp; pattern reported in this infant &nbsp;as an anticipation phenomenon of subsequent &nbsp;onset of infantile spasms.
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Dissertations / Theses on the topic "Miller-Dieker"

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SIGAUDY, SABINE. "Etude clinique, cytogenetique et moleculaire du syndrome de miller-dieker et des lissencephalies de type 1 isolees." Aix-Marseille 2, 1994. http://www.theses.fr/1994AIX20801.

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Deltour, Sophie. "Étude des mécanismes de repression transcriptionnelle utilisés par le produit du gène suppresseur de tumeur HIC1, un candidat pour le syndrome de Miller-Dieker." Lille 1, 2002. https://pepite-depot.univ-lille.fr/RESTREINT/Th_Num/2002/50376-2002-99.pdf.

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HIC1 pour Hypermethylated In Cancer est un gène candidat suppresseur de tumeur. En effet, il est situé en 17p13. 3 une région d'ADN génomique hyperméthylée dans certains types de cancers ou délétée dans des cancers de l'ovaire. Ce gène code pour un facteur de transcription puisqu'il possède dans sa partie carboxyterminale cinq doigts de zinc de type Krüppel C2H2 capables de lier une séquence spécifique d'ADN, associés à un domaine d'interaction protéine/protéine appelé BTB/POZ en N-terminal. D'abord, nous avons montré que HIC1 est un répresseur transcriptionnel. Contrairement à deux autres protéines de la même famille BTB/POZ, BCL-6 et PLZF qui répriment la transcription en recrutant des complexes constitués de SMRT, mSin3A et HDAC, nous avons montré que le domaine BTB/POZ de HIC1 est incapable de recruter ces complexes. De plus, l'utilisation de la Trichostatine (TSA, inhibiteur des HDACS) a montré que ce domaine réprime la transcription sans recruter une activité histone désacétylase. Un crible double hybride en levure a permis d'isoler plusieurs partenaires dont une protéine possédant une activité histone méthyltransférase. Parallèlement, en réalisant un alignement entre les séquences des différentes protéines HIC1 et d'un paralogue HRG22, dans la région centrale, où l'homologie de séquence en acides aminés est faible, deux motifs peptidiques bien conservés entre les espèces ont été mis en évidence. Le motif dégénéré GLDLSKK, proche de la séquence PLDLS présente dans de nombreuses protéines qui fixent le corépresseur CtBP. HIC1 interagit avec CtBP via ce motif GLDLSKK et que cette région centrale est capable de réprimer la transcription indépendamment du domaine BTB/POZ. Pour conclure, HIC1 réprimerait la transcription de deux façons.
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CHEN, CHIA-LI, and 陳嘉莉. "Case Study on Infant Massage for Action Development in Children with Miller-Dieker syndorome." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/rncjqd.

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碩士<br>中臺科技大學<br>文教事業經營研究所<br>105<br>Title:Case Study on Infant Massage for Action Development in Children with Miller-Dieker syndorome Name of Institute:Central Taiwan University of Science and Technology Graduate Institute of Cultural and Educational Management Graduation Time:2017/06 Page:152 Student:Chen, Chia-Li Degree:Master Adviser:Dr. Hung, Chih-Lun Abstract The present study was a case study aiming to investigate the influences of infant massage on motor development of a child with Miller-Dieker syndrome.This single-case research approaching through observations, interviews and information gathering was applied to look into the physiological development and circumstance nowadays of the child with Miller-Dieker syndrome. The subject was a Miller-Dieker syndrome child in a daycare facility from Taichung. The independent variable was infant massage techniques while improvements on motor development as dependent variable and information was gather from the mother. After the intervention of infant massage, the results show:1.The infantile spasm occurred less than five times in a minute. 2.Head lifting angle was over 15 degrees. 3.Being able to sit or prone independently 4.Being able to roll over. 5.No tongue thrust occurred. 6.Being able to grab objects with palms. Other than that, the parent-child relationship was also improved significantly due to the mother had learned techniques of infant massage herself and applied it personally to her child. With this kind of interactions through the help of infant massage, the mother could witness the progresses in motor development of her child and grow up confidence of nurturing child then get to reach the harmony of parent-child interactions. The study results above could provide a reference of promoting infant massage to relative involvements at different stages such as early intervention facilities, medical employees, pre-school day care centers and parents. We look forward to better influences in the future. Key words: Miller-Dieker syndrome, motor development, infant massage, case study
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Book chapters on the topic "Miller-Dieker"

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Chen, Harold. "Miller-Dieker Syndrome." In Atlas of Genetic Diagnosis and Counseling. Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4614-6430-3_157-2.

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Oette, Mark, Marvin J. Stone, Hendrik P. N. Scholl, et al. "Miller-Dieker Syndrome." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_1148.

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Chen, Harold. "Miller-Dieker Syndrome." In Atlas of Genetic Diagnosis and Counseling. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-2401-1_157.

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Oette, Mark, Marvin J. Stone, Hendrik P. N. Scholl, et al. "Miller-Dieker Lissencephaly Syndrome." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_6248.

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"Miller–Dieker Syndrome." In Atlas of Genetic Diagnosis and Counseling. Springer US, 2012. http://dx.doi.org/10.1007/978-1-4614-1037-9_157.

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"Miller-Dieker Syndrome." In Encyclopedia of Genetics, Genomics, Proteomics and Informatics. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6754-9_10430.

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"Miller–Dieker syndrome, n." In Oxford English Dictionary, 3rd ed. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/6162953874.

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Goetzinger, Katherine R., and Alison G. Cahill. "Miller-Dieker Syndrome (17p13.3 Deletion Syndrome)." In Obstetric Imaging: Fetal Diagnosis and Care. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-323-44548-1.00157-1.

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Marques, Natália da Silva Freitas, Franciely Gomes Gonçalves, Gustavo Souza Moretti, et al. "SÍNDROME MILLER- DIEKER: RELATO DE CASO." In SAÚDE DA CRIANÇA E DO ADOLESCENTE: Aspectos Gestacionais, Neonatais e Pediátricos. Stricto Sensu Editora, 2019. http://dx.doi.org/10.35170/ss.ed.9786580261130.21.

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"11.17 Miller-Dieker-Syndrom (Lissenzephalie Typ I)." In Sonographische Fehlbildungsdiagnostik, edited by Michael Entezami, Matthias Albig, Adam Gasiorek-Wiens, and Rolf Becker. Georg Thieme Verlag, 2002. http://dx.doi.org/10.1055/b-0034-60422.

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