scholarly journals An Overview of Iron in Term Breast-Fed Infants

2015 ◽  
Vol 9 ◽  
pp. CMPed.S26572 ◽  
Author(s):  
Wafaa A. Qasem ◽  
James K. Friel

Background Iron is an essential nutrient for normal growth and neurodevelopment of infants. Iron deficiency (ID) remains the most common micronutrient deficiency worldwide. There are convincing data that ID is associated with negative effects on neurological and psychomotor development. Objectives In this review, we provide an overview of current knowledge of the importance of iron in normal term breast-fed infants with a focus on recommendations, metabolism, and iron requirements. Conclusions Health organizations around the world recommend the introduction of iron-rich foods or iron supplements for growing infants to prevent ID. However, there is no routine screening for ID in infancy. Multicenter trials with long-term follow-up are needed to investigate the association between iron fortification/supplementation and various health outcomes.

JAMA Surgery ◽  
2014 ◽  
Vol 149 (12) ◽  
pp. 1266 ◽  
Author(s):  
Hani Y. Hasan ◽  
J. Louis Hinshaw ◽  
Edward J. Borman ◽  
Alison Gegios ◽  
Glen Leverson ◽  
...  

2021 ◽  
Author(s):  
Maria Cristina Vigone ◽  
Rita Ortolano ◽  
Gaia Vincenzi ◽  
Clara Pozzi ◽  
Micol Ratti ◽  
...  

Objective. Oral solution and tablet formulations of Levo-Thyroxine (L-T4) are both used in the treatment of Congenital Hypothyroidism (CH). However, few studies and with a limited follow-up period have been published comparing these two formulations in children. Design. The aim of this multicenter study was to compare the effectiveness of L-T4 oral solution (with ethanol as excipient) and tablet formulation in children with CH up to 3 years of age. Methods. Children diagnosed with CH between 2006 and 2015 were enrolled and divided into two groups according to the L-T4 formulation used: solution in drops (Group D) or tablets (Group T). Auxological parameters, TSH and FT4 values and L-T4 dose were collected at diagnosis and at 15 days, 1, 3, 6, 12, 24 and 36 months of treatment. The Developmental Quotient at 1 and 3 years of age was evaluated using Griffiths’ Scale. Results. 254 children were enrolled. 117 were treated with solution and 137 with tablets. Auxological parameters, dose and thyroid function values at diagnosis, 3, 6, 12, 24, 36 months were not significantly different. TSH at 15 days (p=0.002) and 1 month (p=0.009) was significantly reduced in group D. At 2-year follow-up, median TSH was significantly lower in group T (p=0.03). No statistical difference was detected between the median Developmental Quotient, however group D showed lower values in the language subscale at 12 months and in eye-hand coordination at 36 months. Conclusions. Both therapeutic strategies are effective on treatment of CH. A higher risk of overtreatment in the first months of therapy seems to be associated with oral solution L-T4; therefore, a different strategy should be considered when starting and adjusting the dose. No negative effects in cognitive development were observed. The data obtained are encouraging but long-term follow-up is needed.


2019 ◽  
Vol 45 (1) ◽  
Author(s):  
Carlotta Spagnoli ◽  
Susanna Rizzi ◽  
Grazia Gabriella Salerno ◽  
Daniele Frattini ◽  
Carlo Fusco

Abstract Background Pathogenic variants in KIF1A (kinesin family member 1A) gene have been associated with hereditary spastic paraplegia (HSP) type 30 (SPG30), encopassing autosomal dominant and recessive, pure and complicated forms. Case presentation We report the long-term follow-up of a 19 years-old boy first evaluated at 18 months of age because of toe walking and unstable gait with frequent falls. He developed speech delay, mild intellectual disability, a slowly progressive pyramidal syndrome, microcephaly, bilateral optic subatrophy and a sensory axonal polyneuropathy. Brain MRI showed cerebellar atrophy, stable along serial evaluations (last performed at 18 years of age). Targeted NGS sequencing disclosed the de novo c.914C > T missense, likely pathogenic variant on KIF1A gene. Conclusions We report on a previously unpublished de novo heterozygous likely pathogenic KIF1A variant associated with slowly progressive complicated SPG30 and stable cerebellar atrophy on long-term follow-up, adding to current knowledge on this HSP subtype.


2008 ◽  
Vol 33 (12) ◽  
pp. 1104-1109 ◽  
Author(s):  
Aharon Galil ◽  
Rivka Carmi ◽  
Esther Goldstein ◽  
Basil Porter ◽  
Jacob Bar Ziv ◽  
...  

2005 ◽  
Vol 133 (7-8) ◽  
pp. 343-347
Author(s):  
Slobodan Obradovic ◽  
Andjelka Stojkovic-Andjelkovic ◽  
Biljana Vuletic ◽  
Marija Radovanovic

Brain abscesses were neurosongraphically diagnosed in 3 out of 44 neonates who had confirmed purulent meningitis. In two cases, the cause was Proteus mirabillis, whereas in one the cause could not be isolated. The ultrasound finding indicated abscess cavities localized in the frontal (in one case bilaterally) and temporal regions of the CNS. Neurosurgical interventions were carried out on all of the neonates who had abscesses (including the evacuation of purulent cavity contents, and later on a ventriculoperitoneal shunt in two cases, because of the development of hydrocephalus). Follow-up on the operated infants revealed that one infant died at the age of 9 months; one, who had a bilateral abscess, demonstrated significant neurodevelopmental retardation in the third month of his life (so far it has not been brought under control); while the third one, whom we monitored until the age of 2, displayed regular psychomotor development (preserved intellect, motor skills, sight, and hearing).


1987 ◽  
Vol 5 (7) ◽  
pp. 1098-1106 ◽  
Author(s):  
E E Reynoso ◽  
F A Shepherd ◽  
H A Messner ◽  
H A Farquharson ◽  
M B Garvey ◽  
...  

The incidence of acute leukemia in pregnancy is low and even referral centers have limited experience. Although the short-term risks for children exposed in utero to cytotoxic agents are predictable, there is no information on long-term complications. We report here our experience in the treatment of seven cases of acute leukemia diagnosed during pregnancy, and a literature review of 51 cases published since 1975. Fifty-three patients received chemotherapy during their pregnancies. Forty-nine of the 58 cases resulted in the birth of 50 live infants. Twenty-eight infants were born prematurely, and four had low birth-weights for their gestational age. Thirty-three percent of the newborns exposed to chemotherapy in the last month of pregnancy were cytopenic at birth, but other perinatal complications were not increased. Only one child (present series) had obvious congenital malformations, and this same infant later developed a neuroblastoma arising in the adrenal gland and a papillary carcinoma of the thyroid. Follow-up data are not provided in most previously reported cases, but long-term follow-up of our cases from 1 to 17 years has shown normal growth and development and no further malignancies. A central registry is strongly advised in order to document the long-term complications arising in children exposed to chemotherapy in utero.


Contraception ◽  
1984 ◽  
Vol 30 (6) ◽  
pp. 523-533 ◽  
Author(s):  
Jorge Jimenez ◽  
Margarita Ochoa ◽  
Maria Paz Soler ◽  
Patricio Portales

Author(s):  
Y. Ando ◽  
K. Kakimoto ◽  
M. Deguchi ◽  
T. Naeda ◽  
M. Ohtakara ◽  
...  

2012 ◽  
Vol 29 (5) ◽  
pp. 395-414 ◽  
Author(s):  
Maëlle de Ville de Goyet ◽  
Stéphane Moniotte ◽  
Bénédicte Brichard

2003 ◽  
Vol 46 (3) ◽  
pp. 177-179 ◽  
Author(s):  
Y. Ando ◽  
Y. Matsumoto ◽  
S. Nakano ◽  
K. Saito ◽  
K. Kakimoto ◽  
...  

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