How to Trip Rapid Review

Step 1: Select articles relevant to your search (remember the system is only optimised for single intervention studies)

Step 2: press

Step 3: review the result, and maybe amend the or if you know better! If we're unsure of the overall sentiment of the trial we will display the conclusion under the article title. We then require you to tell us what the correct sentiment is.

167 results for

Infantile Hypothyroidism

by
...
Latest & greatest
Alerts

Export results

Use check boxes to select individual results below

SmartSearch available

Trip's SmartSearch engine has discovered connected searches & results. Click to show

1. Resolution of Consumptive Hypothyroidism Secondary to Infantile Hepatic Hemangiomatosis with a Combination of Propranolol and Levothyroxine (PubMed)

Resolution of Consumptive Hypothyroidism Secondary to Infantile Hepatic Hemangiomatosis with a Combination of Propranolol and Levothyroxine Infantile hepatic hemangiomas (IHH), particularly of the diffuse subtype can, in severe cases, be associated with hepatic and cardiac failure, compartment syndrome and consumptive hypothyroidism. Early recognition and treatment of these pathologies is paramount in order to minimise the risk of long-term sequelae. We report an interesting case of a female (...) infant who presented with systemic compromise, in the absence of large or obvious cutaneous infantile hemangiomas. Imaging identified innumerable hepatic hemangiomas, consistent with diffuse infantile hepatic hemangiomatosis. Subsequent to this, thyroid function tests confirmed an associated but comparatively rare form of hypothyroidism, known as consumptive hypothyroidism. Following joint consultation with dermatology and endocrinology she was promptly treated with oral propranolol and levothyroxine

Full Text available with Trip Pro

2018 Journal of clinical research in pediatric endocrinology

2. Infantile Hypothyroidism

Infantile Hypothyroidism Infantile Hypothyroidism Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Infantile Hypothyroidism Infantile (...) Hypothyroidism Aka: Infantile Hypothyroidism , Neonatal Hypothyroidism , Hypothyroidism in Infants , Cretinism II. Pathophysiology Congenital III. Causes Enzymatic defect Idodine deficiency IV. Signs Dwarfism Yellow dry thick skin Thick lips and Short hands with thick fingers Delayed deciduous Delayed Slow Movement V. Labs See Images: Related links to external sites (from Bing) These images are a random sampling from a Bing search on the term "Infantile Hypothyroidism." Click on the image (or right click

2018 FP Notebook

3. Clinical Practice Guideline for the Management of Infantile Hemangiomas

Clinical Practice Guideline for the Management of Infantile Hemangiomas Clinical Practice Guideline for the Management of Infantile Hemangiomas | From the American Academy of Pediatrics | Pediatrics '); document.write(''); } function OAS_AD(pos) { if (OAS_version >= 11 && typeof(OAS_RICH)!='undefined') { OAS_RICH(pos); } else { OAS_NORMAL(pos); } } //--> Search for this keyword Source User menu Sections Sign up for highlighting editor-chosen studies with the greatest impact on clinical care (...) . Clinical Practice Guideline for the Management of Infantile Hemangiomas Daniel P. Krowchuk , Ilona J. Frieden , Anthony J. Mancini , David H. Darrow , Francine Blei , Arin K. Greene , Aparna Annam , Cynthia N. Baker , Peter C. Frommelt , Amy Hodak , Brian M. Pate , Janice L. Pelletier , Deborah Sandrock , Stuart T. Weinberg , Mary Anne Whelan , SUBCOMMITTEE ON THE MANAGEMENT OF INFANTILE HEMANGIOMAS Abstract Infantile hemangiomas (IHs) occur in as many as 5% of infants, making them the most common

2019 American Academy of Pediatrics

4. Diffuse infantile hepatic haemangioma—how to manage an incidental but potentially lethal finding (PubMed)

Diffuse infantile hepatic haemangioma—how to manage an incidental but potentially lethal finding Infantile hepatic haemangioma (IHH) is a rare vascular tumour that is potentially lethal due to its associated complications, including heart failure, hepatic failure, hypothyroidism and abdominal compartment syndrome. The authors report a case of an asymptomatic diffuse IHH in a newborn male, which was presented as an incidental finding at the time that the patient was diagnosed with pyloric

Full Text available with Trip Pro

2018 Oxford Medical Case Reports

5. Infantile Hypothyroidism

Infantile Hypothyroidism Infantile Hypothyroidism Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Infantile Hypothyroidism Infantile (...) Hypothyroidism Aka: Infantile Hypothyroidism , Neonatal Hypothyroidism , Hypothyroidism in Infants , Cretinism II. Pathophysiology Congenital III. Causes Enzymatic defect Idodine deficiency IV. Signs Dwarfism Yellow dry thick skin Thick lips and Short hands with thick fingers Delayed deciduous Delayed Slow Movement V. Labs See Images: Related links to external sites (from Bing) These images are a random sampling from a Bing search on the term "Infantile Hypothyroidism." Click on the image (or right click

2015 FP Notebook

6. Hypothyroidism in late-onset Pompe disease (PubMed)

Hypothyroidism in late-onset Pompe disease In Pompe disease, a deficiency of acid α-glucosidase enzyme activity leads to pathologic accumulation of glycogen in tissues. Phenotype heterogeneity in Pompe includes an infantile form and late-onset forms (juvenile- and adult-onset forms). Symptoms common to all phenotypes include progressive muscle weakness and worsening respiratory function. Patients with late-onset forms of Pompe disease commonly complain of chronic fatigue and generalized muscle (...) weakness prior to being diagnosed with Pompe disease, and this may lead to consideration of hypothyroidism in the differential diagnosis. This study aimed to evaluate the prevalence of hypothyroidism in the adult-onset form of Pompe disease.Electronic chart review was performed at the Advanced Therapies Clinic at the University of Minnesota Medical Center (UMMC) to identify patients with late-onset Pompe disease. The identified charts were reviewed for a co-diagnosis of hypothyroidism. A query was made

Full Text available with Trip Pro

2016 Molecular genetics and metabolism reports

7. History of the infantile hepatic hemangioma: From imaging to generating a differential diagnosis (PubMed)

History of the infantile hepatic hemangioma: From imaging to generating a differential diagnosis We aim to provide an up-to-date summary of infantile hepatic hemangioma (IHH) and its misnomers and to dialectically present the differential diagnosis of these rare entities of the liver. Eligible peer-reviewed articles on hepatic infantile hemangiomas, published between 2000 and 2015, were reviewed for this study. IHH is the most common hepatic vascular tumor in children. Once a liver mass (...) . Complications can include hepatomegaly, hypothyroidism and cardiac failure. Therefore, a close follow-up is required until complete involution of the lesions. We propose an algorithm to guide the physicians towards the proper management of hepatic lesions.

Full Text available with Trip Pro

2016 World journal of clinical pediatrics

8. A mouse model suggests two mechanisms for thyroid alterations in infantile cystinosis: decreased thyroglobulin synthesis due to endoplasmic reticulum stress/unfolded protein response and impaired lysosomal processing. (PubMed)

A mouse model suggests two mechanisms for thyroid alterations in infantile cystinosis: decreased thyroglobulin synthesis due to endoplasmic reticulum stress/unfolded protein response and impaired lysosomal processing. Thyroid hormones are released from thyroglobulin (Tg) in lysosomes, which are impaired in infantile/nephropathic cystinosis. Cystinosis is a lysosomal cystine storage disease due to defective cystine exporter, cystinosin. Cystinotic children develop subclinical and then overt (...) hypothyroidism. Why hypothyroidism is the most frequent and earliest endocrine complication of cystinosis is unknown. We here defined early alterations in Ctns(-/-) mice thyroid and identified subcellular and molecular mechanisms. At 9 months, T4 and T3 plasma levels were normal and TSH was moderately increased (∼4-fold). By histology, hyperplasia and hypertrophy of most follicles preceded colloid exhaustion. Increased immunolabeling for thyrocyte proliferation and apoptotic shedding indicated accelerated

Full Text available with Trip Pro

2015 Endocrinology

9. Prednisolone Versus Vigabatrin in the First-line Treatment of Infantile Spasms

Prednisolone Versus Vigabatrin in the First-line Treatment of Infantile Spasms Prednisolone Versus Vigabatrin in the First-line Treatment of Infantile Spasms - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more (...) . Prednisolone Versus Vigabatrin in the First-line Treatment of Infantile Spasms (PREDVGB) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT02299115 Recruitment Status : Recruiting First Posted : November 24, 2014 Last Update

2014 Clinical Trials

10. Infantile Hemangioma (Treatment)

. 131(4):643-6. . Ceisler EJ, Santos L, Blei F. Periocular hemangiomas: what every physician should know. Pediatr Dermatol . 2004 Jan-Feb. 21(1):1-9. . Esterly NB. Kasabach-Merritt syndrome in infants. J Am Acad Dermatol . 1983 Apr. 8(4):504-13. . Ersoy S, Mancini AJ. Hemifacial infantile hemangioma with intracranial extension: a rare entity. Pediatr Dermatol . 2005 Jul-Aug. 22(4):309-13. . Huang SA, Tu HM, Harney JW, et al. Severe hypothyroidism caused by type 3 iodothyronine deiodinase (...) in infantile hemangiomas. N Engl J Med . 2000 Jul 20. 343(3):185-9. . Konrad D, Ellis G, Perlman K. Spontaneous regression of severe acquired infantile hypothyroidism associated with multiple liver hemangiomas. Pediatrics . 2003 Dec. 112(6 Pt 1):1424-6. . Ho J, Kendrick V, Dewey D, Pacaud D. New insight into the pathophysiology of severe hypothyroidism in an infant with multiple hepatic hemangiomas. J Pediatr Endocrinol Metab . 2005 May. 18(5):511-4. . North PE, Waner M, Mizeracki A, et al. A unique

2014 eMedicine.com

11. Infantile Hemangioma (Overview)

extension: a rare entity. Pediatr Dermatol . 2005 Jul-Aug. 22(4):309-13. . Huang SA, Tu HM, Harney JW, et al. Severe hypothyroidism caused by type 3 iodothyronine deiodinase in infantile hemangiomas. N Engl J Med . 2000 Jul 20. 343(3):185-9. . Konrad D, Ellis G, Perlman K. Spontaneous regression of severe acquired infantile hypothyroidism associated with multiple liver hemangiomas. Pediatrics . 2003 Dec. 112(6 Pt 1):1424-6. . Ho J, Kendrick V, Dewey D, Pacaud D. New insight into the pathophysiology (...) Infantile Hemangioma (Overview) Infantile Hemangioma: Practice Essentials, Background, Pathophysiology Edition: No Results No Results Please confirm that you would like to log out of Medscape. If you log out, you will be required to enter your username and password the next time you visit. https://profreg.medscape.com/px/getpracticeprofile.do?method=getProfessionalProfile&urlCache=aHR0cHM6Ly9lbWVkaWNpbmUubWVkc2NhcGUuY29tL2FydGljbGUvMTA4Mzg0OS1vdmVydmlldw== processing > Infantile Hemangioma

2014 eMedicine.com

12. Infantile Hemangioma (Follow-up)

. 131(4):643-6. . Ceisler EJ, Santos L, Blei F. Periocular hemangiomas: what every physician should know. Pediatr Dermatol . 2004 Jan-Feb. 21(1):1-9. . Esterly NB. Kasabach-Merritt syndrome in infants. J Am Acad Dermatol . 1983 Apr. 8(4):504-13. . Ersoy S, Mancini AJ. Hemifacial infantile hemangioma with intracranial extension: a rare entity. Pediatr Dermatol . 2005 Jul-Aug. 22(4):309-13. . Huang SA, Tu HM, Harney JW, et al. Severe hypothyroidism caused by type 3 iodothyronine deiodinase (...) in infantile hemangiomas. N Engl J Med . 2000 Jul 20. 343(3):185-9. . Konrad D, Ellis G, Perlman K. Spontaneous regression of severe acquired infantile hypothyroidism associated with multiple liver hemangiomas. Pediatrics . 2003 Dec. 112(6 Pt 1):1424-6. . Ho J, Kendrick V, Dewey D, Pacaud D. New insight into the pathophysiology of severe hypothyroidism in an infant with multiple hepatic hemangiomas. J Pediatr Endocrinol Metab . 2005 May. 18(5):511-4. . North PE, Waner M, Mizeracki A, et al. A unique

2014 eMedicine.com

13. Infantile Hemangioma (Diagnosis)

extension: a rare entity. Pediatr Dermatol . 2005 Jul-Aug. 22(4):309-13. . Huang SA, Tu HM, Harney JW, et al. Severe hypothyroidism caused by type 3 iodothyronine deiodinase in infantile hemangiomas. N Engl J Med . 2000 Jul 20. 343(3):185-9. . Konrad D, Ellis G, Perlman K. Spontaneous regression of severe acquired infantile hypothyroidism associated with multiple liver hemangiomas. Pediatrics . 2003 Dec. 112(6 Pt 1):1424-6. . Ho J, Kendrick V, Dewey D, Pacaud D. New insight into the pathophysiology (...) Infantile Hemangioma (Diagnosis) Infantile Hemangioma: Practice Essentials, Background, Pathophysiology Edition: No Results No Results Please confirm that you would like to log out of Medscape. If you log out, you will be required to enter your username and password the next time you visit. https://profreg.medscape.com/px/getpracticeprofile.do?method=getProfessionalProfile&urlCache=aHR0cHM6Ly9lbWVkaWNpbmUubWVkc2NhcGUuY29tL2FydGljbGUvMTA4Mzg0OS1vdmVydmlldw== processing > Infantile Hemangioma

2014 eMedicine.com

14. Epidemiology and Clinical Characteristics of Congenital Hypothyroidism in an Asian Population: A Nationwide Population-Based Study (PubMed)

Epidemiology and Clinical Characteristics of Congenital Hypothyroidism in an Asian Population: A Nationwide Population-Based Study The incidence of congenital hypothyroidism (CH) has been increasing in Western countries, and some populations, including Asians, have a higher incidence. Delayed diagnosis and early treatment influence the outcome of CH. We investigated the incidence and clinical characteristics of CH in Taiwan.In this retrospective database study we identified cases of CH (...) 10 000 births. Among 1115 patients, the most common clinical features of CH were developmental delay (9.6%), constipation (11.6%), and delayed physiological development (9.1%). Congenital anomalies of the heart (7.7%), epilepsy (2.7%), and infantile cerebral palsy (3.2%) were also noted. Survival analysis showed that the risks of mental retardation (hazard ratio [HR], 3.180) and delayed physiological development (HR, 1.908) were greater when age at diagnosis was greater than 1 year.CH incidence

Full Text available with Trip Pro

2013 Journal of Epidemiology

15. Transient infantile hyperthyrotropinaemia. Report of a case. (PubMed)

Transient infantile hyperthyrotropinaemia. Report of a case. A case of transient hyperthyrotropinaemia was found by mass screening for neonatal hypothyroidism using the paired TSH assay method. The patient was a baby boy born at term after a normal pregnancy who grew without any abnormal signs or symptoms. For the first 7 months after birth, his serum TSH was abnormally high while his total serum T4, T3, and free T4, T3 were within normal limits, exept for slightly low free T4 level at 7 months

Full Text available with Trip Pro

1979 Archives of Disease in Childhood

16. Prepregnancy counseling

, and renal disease for women with longstanding or uncontrolled hypertension. y – Hypothyroidism (untreated) Spontaneous abortion, preeclampsia, preterm birth, placental abruption, and fetal death Screening based on risk factors, rather than universal screening, should be considered for patients who are planning pregnancy. y,z Treat if thyrotropin (previously thyroid-stimulating hormone) is abovetheupperlevelofnormal. Bariatric surgery A period of rapid weight loss typicallyoccursinthe?rst12–24 months (...) Association Taskforce on Hypothyroidism in Adults. [published errata appear in Thyroid 2013;23:251; Thyroid 2013;23:129]. Thyroid 2012;22:1200–35. z Subclinical hypothyroidism in the infertile female population: a guideline. Practice Committee of the American Society for Reproductive Medicine. Fertil Steril 2015;104:545–53. x Bariatric surgery and pregnancy. ACOG Practice Bulletin No. 105. American College of Obstetricians and Gynecologists. Obstet Gynecol 2009;113:1405–13. jj Casilla-Lennon MM, Meltzer

2019 Society for Assisted Reproductive Technology

17. CRACKCast E172 – Pediatric Gastrointestinal Disorders

jaundice (>50% of cases of jaundice!) Onset at 2-7 days of life. Breast milk jaundice (2nd most common cause) Hormonally mediated or related to increased enterohepatic reabsorption of bilirubin. Typically presents after the first three to five days of life, peaking within two weeks after birth Hemolysis: ABO incompat. Cephalohematoma Breakdown diseases: spherocytosis, thalassemia, G6PD Obstructive: Meconium ileus Pyloric stenosis Infectious Metabolic Congenital hypothyroidism [2] List indications (...) of NEC is unclear but is likely multifactorial. Prematurity is the most common and universally accepted risk factor; 90% of all affected infants are born prematurely. The primary pathologic event may be inflammation or injury to the intestinal wall, beginning in the mucosa and extending transmurally. [3] List five pathologic causes of constipation in a child. Neurogenic Hirschsprung’s disease CP Spinal cord injury Neurofibromatosis Infantile botulism Dysautonomia Duchenne muscular dystrophy Endocrine

2018 CandiEM

18. Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting

recommend a formal audiometric evaluation every 5 years regardless of the initial age at diagnosis, initial hearing threshold levels, karyotype and/or presence of a mid-frequency sensorineural hearing loss, to assure early and adequate technical and other rehabilitative measures (⨁⨁◯◯). R 6.2. We recommend aggressive treatment of middle-ear disease and otitis media (OM) with antibiotics and placement of myringotomy tubes as indicated (⨁⨁◯◯). R 6.3. We recommend screening for hypothyroidism at diagnosis (...) facial appearance, with neck webbing and lymphedema ( , ), we suggest that the clinical manifestations of TS should be broadened to include other features, such as linear growth failure, ovarian insufficiency (pubertal delay), early sensorineural hearing loss, distinctive congenital cardiovascular, skeletal, digital and renal anomalies, a particular neurodevelopmental profile, and a constellation of other disorders that are more common in TS, including hypothyroidism and celiac disease ( , , ). Table

Full Text available with Trip Pro

2016 European Society of Human Reproduction and Embryology

20. Guideline for the Evaluation of Cholestatic Jaundice in Infants: Joint Recommendations of NASPGHAN and ESPGHAN

liver disease, metabolic disease, or sepsis. When evaluating a patient with cholestasis, it is crucial to review the standard local newborn screening as many diseases that cause cholestasis are tested such as hypothyroidism, galactosemia, tyr- osinemia, and CF. Some countries have extended newborn screens that can be performed upon request. The minimum evaluation for any health care professional encountering an infant with jaundice present after the age of 14 days should include a full history (...) screen results not readily available Urine—urinalysis, culture, reducing substances (rule out galactosemia) Consider bacterial cultures of blood, urine and other ?uids especially if infant is clinically ill. Verify results of treatable disorders (such as galactosemia and hypothyroidism) from newborn screen Obtain fasting ultrasound Tier 2: Aim to complete a targeted evaluation in concert with pediatric gastroenterologist/hepatologist General—TSH and T4 values, serum bile acids, cortisol Consideration

2017 North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition

To help you find the content you need quickly, you can filter your results via the categories on the right-hand side >>>>