Zobrazeno 1 - 10
of 11 222
pro vyhledávání: '"congenital malformations"'
Autor:
Cristiane S. R. Fonteles, Julia Enterria-Rosales, Ying Lin, John W. Steele, Ramiro A. Villarreal-Leal, Jing Xiao, Daniel I. Idowu, Beck Burgelin, Bogdan J. Wlodarczyk, Richard H. Finnell, Bruna Corradetti
Publikováno v:
Stem Cell Research & Therapy, Vol 15, Iss 1, Pp 1-15 (2024)
Abstract Background: Mesenchymal stem cells (MSCs) derived from gestational tissues offer a promising avenue for prenatal intervention in congenital malformations although their application is hampered by concerns related to cellular plasticity and t
Externí odkaz:
https://doaj.org/article/a0c549808a4a4dd784984e6c81c1b25a
Autor:
D. O. Ivanov, S. A. Fomin, K. V. Pshenisnov, Yu. S. Aleksandrovich, L. V. Ditkovskaya, A. M. Fomin
Publikováno v:
Вестник анестезиологии и реаниматологии, Vol 21, Iss 4, Pp 69-77 (2024)
Introduction. Adrenal insufficiency is often found in critical conditions of the neonatal period and has nonspecific symptoms, which greatly complicates its diagnosis. The objective was to study the hormonal status of newborns with congenital malform
Externí odkaz:
https://doaj.org/article/815c37fee5be434d8824c552616d9455
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Background The MACF1 gene, found on chromosome 1p34.3, is vital for controlling cytoskeleton dynamics, cell movement, growth, and differentiation. It consists of 101 exons, spanning over 270 kb. The 16p13.11 microduplication syndrome results
Externí odkaz:
https://doaj.org/article/59b165c410704e1fae2de1f299bd75f5
Publikováno v:
Nigerian Journal of Paediatrics, Vol 32, Iss 2, Pp 47-51 (2024)
Background: The prevalence of congenital malformations varies from place to place. With a declining economy, increased utilization of traditional medications, and the traditional culture of consanguinity in Kano area, we decided to examine the incide
Externí odkaz:
https://doaj.org/article/6be6e8c809b84e5c9c5053e701338392
Autor:
A.O. Ifesanya, B.A. Omololu
Publikováno v:
Nigerian Journal of Paediatrics, Vol 38, Iss 2, Pp 95-99 (2024)
Proximal focal femoral deficiency (PFFD) is a rare but often severe abnormality of the lower limb which poses a significant challenge to effective treatment. We reviewed 21 patients with 23 cases of PFFD treated in our centre in the 14-year period fr
Externí odkaz:
https://doaj.org/article/fd393abafac74148a2d5f813ad044d43
Autor:
Ifesanya AO, Omololu BA
Publikováno v:
Nigerian Journal of Paediatrics, Vol 39, Iss 2, Pp 75-78 (2024)
Proximal focal femoral deficiency (PFFD) is a rare but often severe abnormality of the lower limb which poses a significant challenge to effective treatment. We reviewed 21 patients with 23 cases of PFFD treated in our centre in the 14-year period fr
Externí odkaz:
https://doaj.org/article/548e0a388dfb4171808752da345a548f
Autor:
Onankpa BO, Adamu A
Publikováno v:
Nigerian Journal of Paediatrics, Vol 41, Iss 4, Pp 337-340 (2024)
Background: Congenital malformation(s) do occur in newborns and are thought to be often responsible for a significant proportion of perinatal morbidity and mortality worldwide. Objective: This prospective study was designed to determine the patter
Externí odkaz:
https://doaj.org/article/3b8e5d1d23ca439ca0b1db2d449e63d0
Publikováno v:
Nigerian Journal of Paediatrics, Vol 45, Iss 1, Pp 19-24 (2024)
This report is on holoprosencephaly (HPE) sequence with other clinical and radiographic anomalies of other organs. This condition which has never been reported in Yenagoa, an oil rich Niger Delta Region was observed simultaneously in two neonates wit
Externí odkaz:
https://doaj.org/article/19ff0aa2ce644f6e8f8d55694e1c26ce
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-7 (2024)
Abstract It is crucial to create a cost-effective work protocol that will guide everyone involved in diagnosing children with dysmorphic features step-by-step and ensure that testing costs are reduced without compromising care quality in light of the
Externí odkaz:
https://doaj.org/article/c89a6e20dcf0433f83c8dda986033fd0
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 16, Iss 3, Pp 4-11 (2024)
There are currently about 15 million women of childbearing age worldwide who suffer from epilepsy. Overall, 0.3–0.4% of newborns are born to mothers with epilepsy, and almost half of these women experience recurrent seizures. The article discusses
Externí odkaz:
https://doaj.org/article/4abf88453ec9467a906c383d0ad99c21