Deficiencia de la hormona del crecimiento pdf




















Diversos estudios han demostrado que el uso de HChr a dosis de 0. Sin embargo, una vez realizado el trasplante renal, el uso de glucocorticoides en dosis elevadas puede disminuir o incluso neutralizar el efecto de HChr sobre la velocidad de crecimiento, por lo que la estatura final lograda suele ser menor a la esperada para la familia. No se ha observado una mayor incidencia de rechazos al trasplante con el uso de HChr. El uso de HChr a dosis de 0.

Se debe mantener el crecimiento hasta que se logre una estatura final o casi final. El uso de HChr en dosis de 0. Si durante el brote de crecimiento de la pubertad se observa una velocidad de crecimiento menor a la centila 25, se debe reiniciar el manejo hasta que se termina la fase ascendente del pico de crecimiento asociado a la pubertad. Raben MS. Treatment of a pituitary dwarf with human growth hormone. J Clin Endocrinol Metab. Sexual ateliotic dwarfism: A recessively inherited isolated deficiency of growth hormone.

Trans Assoc Am Phys. General Tom Thumb and other midgets. Sci Am. Frasier SD. The not-so-good old days: Working with pituitary growth hormone in North America, to J Pediatr. Cronin MJ. Pioneering recombinant growth hormone manufacturing: Pounds produced per mile of height.

Lindholm J. Growth hormone: historical notes. Estimated cost-effectiveness of growth hormone therapy for idiopathic short stature. Arch Pediatr Adolesc Med. Richmond E, Rogol AD. Current indications for growth hormone therapy for children and adolescents. Endocr Dev. Gupta V. Adult growth hormone deficiency.

Indian J Endocrinol Metab. Ayyar VS. History of growth hormone therapy. Genetic Engineering Tech Internet. San Francisco, Ca. Citado 4 abril Cohen LE. Springer International Publishing Switzerland. Bol Med Hosp Infant Mex. Recombinant human growth hormone for the treatment of growth disorders in children: a systematic review and economic evaluation. Health Technol Assess. Porter ME. What is value in health care? N Engl J Med. Growth hormone treatment in non-growth hormone-deficient children.

Ann Pediatr Endocrinol Metab. National Institute for Health and Clinical Excellence: Human growth hormone Somatotropin for the treatment of growth failure in children. NICE technology appraisal guidance. Burden of growth hormone deficiency and excess in children. Prog Mol Biol Transl Sci. Arch Dis Childhood. Clin Endocrinol. Derivation and validation of a mathematical model for predicting the response to exogenous recombinant human growth hormone GH in prepubertal children with idiopathic GH deficiency.

The potential of prediction models based on data from KIGS as tools to measure responsiveness to growth hormone. Horm Res ;55 Suppl 2 Generalidades del uso de hormona de crecimiento. Ranke MB, Lindberg A. Observed and predicted growth responses in prepubertal children with growth disorders: Guidance of growth hormone treatment by empirical variables.

Growth plate senescence and catch-up growth. Endoc Dev. How to optimally manage growth hormone therapy: Survey of chilean pediatric endocrinologists. Horm Res Paediatr. Validation of prediction models for near adult height in children with idiopathic growth hormone deficiency treated with growth hormone: A Belgian registry study.

Horm Res. The growth hormone cascade: progress and long-term results of growth hormone treatment in growth hormone deficiency. Mullis PE. Genetics of isolated growth hormone deficiency. J Clin Res Pediatr Endocrinol. Septo-optic dysplasia. Eur J Hum Genet. Septo-optic dysplasia: antenatal risk factors and clinical features in a regional study. Isolated growth hormone deficiency in two siblings because of paternal mosaicism for a mutation in the GH1 gene.

Genotypic and phenotypic analysis of individuals with mutations in Sonic Hedgehog. J Med Genet. The use of neuroimaging for assessing disorders of pituitary development. Clin Pediatr Endocrinol.

Splice site mutations in GH1 detected in previously genetically undiagnosed families with congenital isolated growth hormone deficiency type II. Molecular genetic studies in isolated growth hormone deficiency IGHD. Indian J Pediatr. Berio A, Piazzi A. Multiple endocrinopathies growth hormone deficiency, autoimmune hypothyroidism and diabetes mellitus in Kearns-Sayre syndrome.

Pediatr Med Chir ;— Isolated growth hormone deficiency GHD in childhood and adolescence: recent advances. Endocr Rev. Familiar isolated growth hormone deficiency due to a novel homozygous missense mutation in the growth hormone releasing hormone receptor gene: Clinical presentation with hypoglycemia. Whole exome sequencing to identify genetic causes of short stature. Novel mutations in the GH gene GH1 uncover putative splicing regulatory elements.

Barnes N, Chemaitilly W. Endocrinopathies in survivors of childhood neoplasia. Front Pediatr. Prevalence of pituitary dysfunction after severe traumatic brain injury in children and adolescents: A large prospective study. Prevalence of posttraumatic growth hormone deficiency is highly dependent on the diagnostic set-up: Results from The Danish National Study on Posttraumatic Hypopituitarism.

Is routine endocrine evaluation necessary after paediatric traumatic brain injury? J Endocrinol Invest. A novel heterozygous SOX2 mutation causing congenital bilateral anophthalmia, hypogonadotropic hypogonadism and growth hormone deficiency. Molecular screening of a large cohort of moroccan patients with congenital hypopituitarism.

Anterior hypopituitarism in adult survivors of childhood cancers treated with cranial radiotherapy: A report from the St Jude Lifetime Cohort Study. J Clin Oncol. Early endocrine alterationsreflect prolonged stress and relate to one year functional outcome in patients with severe braininjury. Eur J Endocrinol. New insights into genotype-phenotype correlation for GLI3 mutations. El Sistema de la Hormona de Crecimiento. A critical evaluation of bioimpedance-spectroscopy analysis in estimating body composition during GH treatment: Comparison with bromide dilution and dual X-ray absorptiometry.

Factors determining pubertal growth and final height in growth hormone treatment of idiopathic growth hormone deficiency. Acta Paediatr. Bajpai A, Menon PS. Growth hormone therapy. Effect of growth hormone GH treatment on the near-final height of patients with idiopathic GH deficiency: Analysis of a large international database.

Fifteen years of GH replacement improves body composition and cardiovascular risk factors. The influence of growth hormone treatment on glucose homeostasis in growth hormone deficient children.

Growth hormone deficiency: Transition from adolescence to adulthood. J Pediatric Endocrinol Metab. Bondy CA. Turner Syndrome Study Group. Davenport ML. Approach to the patient with Turner syndrome. Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome.

Nat Genet. Prepubertal girls with Turner syndrome and children with isolated SHOX deficiency have similar bone geometry at the radius. Prediction of long-term response to recombinant human growth hormone in Turner syndrome: Development and validation of mathematical models. Stephure DK. Canadian Growth Hormone Advisory Committee. Impact of growth hormone supplementation on adult height in turner syndrome: results of the Canadian randomized controlled trial.

Recombinant growth hormone for children and adolescents with Turner syndrome. Cochrane Database Syst Rev. Growth hormone treatment of early growth failure in toddlers with Turner syndrome: A randomized, controlled, multicenter trial.

Growth hormone treatment before the age of 4 years prevents short stature in young girls with Turner syndrome. A critical appraisal of growth hormone therapy in growth hormone deficiency and Turner syndrome patients in Turkey. Las manifestaciones, si las hay, son prematurez, retraso del crecimiento intrauterino, ictericia, hepatoesplenomegalia La deficiencia de hormona de crecimiento normalmente se manifiesta como falta de crecimiento, a veces junto con retraso en el desarrollo de los dientes.

Condiciones inflamatorias e inmunes p. La respuesta de la GH que se considera normal es algo arbitraria. Ocurre en todo el mundo y se presenta de varias formas y subtipos. El cortisol ver Tratamiento Tratamiento La enfermedad de Addison es un trastorno hipofuncionante insidioso y en general progresivo de la corteza suprarrenal. Puede desencadenar una crisis suprarrenal con colapso cardiovascular.

La deficiencia de GH provoca baja estatura; numerosas otras manifestaciones pueden estar presentes dependiendo de la causa. WHO: Growth charts for children 0 to 2 years. CDC: Growth charts for children 2 years and older.

Drug and Therapeutics Committee and Ethics Committee of the Pediatric Endocrine Society: Guidelines for growth hormone and insulin-like growth factor-1 treatment in children and adolescents: Growth hormone deficiency, idiopathic short stature, and primary insulin-like growth factor-I deficiency.



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