Cargando…

Recombinant growth hormone therapy in a girl with costello syndrome: a 4-year observation

BACKGROUND: Costello syndrome is a rare syndrome of multiple congenital anomalies. The typical clinical traits include dysmorphic craniofacial features, skin hyperpigmentation and excess, feeding difficulties leading to severe postnatal growth retardation, short stature, joint hypermobility, and del...

Descripción completa

Detalles Bibliográficos
Autores principales:	Blachowska, Ewa, Petriczko, Elżbieta, Horodnicka-Józwa, Anita, Skórka, Agata, Pelc, Magdalena, Krajewska-Walasek, Małgorzata, Walczak, Mieczysław
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2016
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4729164/ https://www.ncbi.nlm.nih.gov/pubmed/26812928 http://dx.doi.org/10.1186/s13052-015-0209-4

Ejemplares similares

The influence of maternal nutritional behaviour on the nutritional behaviour of children with excess body weight
por: Strączek, Kamilla, et al.
Publicado: (2021)

Nonalcoholic fatty liver disease in children with obesity– observations from one clinical centre in the Western Pomerania region
por: Marcinkiewicz, Katarzyna, et al.
Publicado: (2022)

Impact of One-Year Dietary Education on Change in Selected Anthropometric and Biochemical Parameters in Children with Excess Body Weight
por: Strączek, Kamilla, et al.
Publicado: (2022)

Effects of 12-Month Interdisciplinary Interventions in 8- and 9-Year-Old Children with Excess Body Weight
por: Raducha, Dominika, et al.
Publicado: (2022)

Familial dietary intervention in children with excess body weight and its impact on eating habits, anthropometric and biochemical parameters
por: Strączek, Kamilla, et al.
Publicado: (2022)

Ellizabeth Costello /
por: Coetzee, J. M., 1940-
Publicado: (2004)

Permanent and transient congenital hypothyroidism in full-term and preterm born infants
por: Petriczko, Elżbieta, et al.
Publicado: (2013)

An Interview with Julia G. Costello
por: Farris, Glenn J.
Publicado: (2021)

Hypertrophic scars in a patient with Turner's syndrome treated with recombinant growth hormone
por: Kędzia, Andrzej, et al.
Publicado: (2014)

Assessment of Biochemical Parameters in 8- and 9-Year-Old Children with Excessive Body Weight Participating in a Year-Long Intervention Program
por: Raducha, Dominika, et al.
Publicado: (2023)

The Impact of Growth Hormone Therapy on the Apoptosis Assessment in CD34+ Hematopoietic Cells from Children with Growth Hormone Deficiency
por: Kawa, Miłosz Piotr, et al.
Publicado: (2017)

Anterior lenticular opacities in Costello Syndrome
por: Thakur, Anchal, et al.
Publicado: (2021)

Association of functional genetic variants of A-kinase anchoring protein 10 with QT interval length in full-term Polish newborns
por: Łoniewska, Beata, et al.
Publicado: (2013)

Syndrome de Costello: à propos d'une observation
por: Tajir, Mariam, et al.
Publicado: (2012)

Recombinant GH treatment in a case of Costello syndrome with a 5-year follow-up
por: Kizilcan Cetin, Sirmen, et al.
Publicado: (2020)

Costello Syndrome: The Challenge of Hypoglycemia and Failure to Thrive
por: Leoni, C., et al.
Publicado: (2017)

Treatment of Dystonia Using Trihexyphenidyl in Costello Syndrome
por: Romeo, Domenico M., et al.
Publicado: (2020)

Multidisciplinary Management of Costello Syndrome: Current Perspectives
por: Leoni, Chiara, et al.
Publicado: (2022)

Spectrum of JAG1 gene mutations in Polish patients with Alagille syndrome
por: Jurkiewicz, Dorota, et al.
Publicado: (2014)

Response to Treatment with Recombinant Human Growth Hormone (rhGH) of Short Stature Children Born Too Small for Gestational Age (SGA) in Selected Centres in Poland
por: Glińska, Marta, et al.
Publicado: (2022)

Craniofacial and cutaneous findings in Noonan, Costello and LEOPARD syndromes
por: Pokrowiecki, Rafał, et al.
Publicado: (2018)

Fatal leukodystrophy in Costello syndrome: a case report
por: Failoc-Rojas, Virgilio E., et al.
Publicado: (2023)

Rapid Weight Loss and Severe Failure to Thrive Mimicking Lipodystrophy Syndrome in a 1-Year-Old Taiwanese Girl with Costello Syndrome
por: Syu, Yu-Min, et al.
Publicado: (2022)

The Predictors of Obesity among Urban Girls and Boys Aged 8–10 Years—A Cross-Sectional Study in North-Western Poland
por: Ratajczak, Joanna, et al.
Publicado: (2020)

Difficulties in Interpreting IGF-1 Levels in Short Stature Children Born Small for Gestational Age (SGA) Treated with Recombinant Human Growth Hormone (rhGH) Based on Data from Six Clinical Centers in Poland
por: Glińska, Marta, et al.
Publicado: (2023)

Effect of switching recombinant human growth hormone: Comparative analysis of phase 3 clinical data
por: Romer, Tomasz, et al.
Publicado: (2011)

Correlation of Genotype and Perinatal Period, Time of Diagnosis and Anthropometric Data before Commencement of Recombinant Human Growth Hormone Treatment in Polish Patients with Prader–Willi Syndrome
por: Lecka-Ambroziak, Agnieszka, et al.
Publicado: (2021)

Cytotoxicity of Zardaverine in Embryonal Rhabdomyosarcoma from a Costello Syndrome Patient
por: Cartledge, Donna M., et al.
Publicado: (2017)

Effects of Recombinant Human Growth Hormone Treatment, Depending on the Therapy Start in Different Nutritional Phases in Paediatric Patients with Prader–Willi Syndrome: A Polish Multicentre Study
por: Lecka-Ambroziak, Agnieszka, et al.
Publicado: (2021)

Skeletal defects and bone metabolism in Noonan, Costello and cardio-facio-cutaneous syndromes
por: Papadopoulou, Anna, et al.
Publicado: (2023)

Life-threatening cardiac episode in a Polish patient carrying contiguous gene microdeletion of the TBX5 and the TBX3 genes
por: Iwanicka-Pronicka, Katarzyna, et al.
Publicado: (2016)

Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes
por: Kratz, C P, et al.
Publicado: (2015)

Dysregulated ECM remodeling proteins lead to aberrant osteogenesis of Costello syndrome iPSCs
por: Choi, Jong Bin, et al.
Publicado: (2021)

Concurrent Presentation of Euryblepharon and Moyamoya Syndrome in Costello Syndrome: A Rare Clinical Case
por: Alhazmi, Asma M, et al.
Publicado: (2023)

The Splicing Efficiency of Activating HRAS Mutations Can Determine Costello Syndrome Phenotype and Frequency in Cancer
por: Hartung, Anne-Mette, et al.
Publicado: (2016)

Costello Syndrome and Umbilical Ligament Rhabdomyosarcoma in Two Pediatric Patients: Case Reports and Review of the Literature
por: Sánchez-Montenegro, Carlos, et al.
Publicado: (2017)

Precocious puberty and Chiari I malformation with syrinx: a case report of an unusual presentation of Costello syndrome
por: Schwartz, Naomi S., et al.
Publicado: (2019)

Musculo-skeletal phenotype of Costello syndrome and cardio-facio-cutaneous syndrome: insights on the functional assessment status
por: Leoni, Chiara, et al.
Publicado: (2021)

HRAS germline mutations impair LKB1/AMPK signaling and mitochondrial homeostasis in Costello syndrome models
por: Dard, Laetitia, et al.
Publicado: (2022)

Increased osteoclastogenesis contributes to bone loss in the Costello syndrome Hras G12V mouse model
por: Nandi, Sayantan, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_8r3bsebqi47vlp4fpf61nb4k0u