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343 Possible Causes for Early Onset Puberty, Pediatric Disorder, Vomiting

  • Diabetes Mellitus Type 1

    […] cramping Skin infections Emergency diabetes symptoms Seek urgent medical attention if diabetes symptoms combine with any of the following: A serious loss of appetite Nausea and vomiting[diabetes.co.uk] Adult and pediatric endocrinologists, specialists in treating hormonal disorders and disorders of the endocrine system, manage patients with diabetes.[medicinenet.com] Type 1 DM usually starts in children aged 4 years or older, appearing fairly abruptly, with the peak incidence of onset at age 11-13 years (ie, in early adolescence and puberty[emedicine.medscape.com]

  • Anorexia Nervosa

    During admission her vomiting worsened and she developed visual hallucinations and confabulation.[ncbi.nlm.nih.gov] Identifying and treating eating disorders. Pediatrics. 2003;111:204-11. ).[acphospitalist.org] […] as age 8 and as late as middle age, but its onset is most common around or just after puberty.[emilyprogram.com]

  • Abdominal Migraine

    Vomiting and abdominal pain are symptoms that may arise from a number of different causes.[ncbi.nlm.nih.gov] Abdominal migraine, primarily a pediatric disorder, is often under diagnosed and misunderstood as it can mimic several other systemic and often potentially dangerous clinical[medcraveonline.com] The onset of stomach migraines is most commonly seen in the early childhood years.[tummytrouble.co.uk]

  • Fabry Disease

    Non-specific gastrointestinal symptoms, including pain, diarrhoea, nausea, and vomiting, can be the first symptoms of Fabry disease.[ncbi.nlm.nih.gov] , and the Society for Pediatric Research.[books.google.de] Often patients have slight builds with characteristic coarse facial features and delayed puberty.[patient.info]

  • Erythropoietic Coproporphyria

    Episodes of acute porphyria can cause abdominal pain, vomiting, constipation, and diarrhea.[icdlist.com] Tortorelli S, Kloke K, Raymond K: Chapter 15: Disorders of porphyrin metabolism. In Biochemical and Molecular Basis of Pediatric Disease. Fourth edition.[mayomedicallaboratories.com] […] after puberty Erythropoietic protoporphyria Early childhood with edema and erythema Chronic stages present with scarring and cobblestone thickening of the dorsum of hands[thedoctorsdoctor.com]

  • Systemic Mastocytosis

    The most frequent adverse events were low-grade nausea, vomiting, and diarrhea.[ncbi.nlm.nih.gov] In Romania, the number of the diagnosed patients with mast cell disorders is 252, of which 180 adults and 73 pediatric patients.[medichub.ro] A childhood onset form is distinguished from the adult onset form by its early appearance (usually within the first year of life) and good prognosis with spontaneous resolution[worldallergy.org]

  • Mumps

    A 66-year-old Chinese man presented to our department with a 1-month speech barrier and 1 day of vomiting.[ncbi.nlm.nih.gov] […] vol. 19 (pg. 1127 - 34 ) 36 Risk of Guillain-Barré syndrome after measles-mumps-rubella vaccination, J Pediatr, 2001, vol. 138 (pg. 250 - 4 ) 37 Neurologic disorders after[doi.org] Children who haven't had mumps, and were not vaccinated in early childhood, should be given the vaccine before they reach puberty.[mydr.com.au]

  • Hemophilia B

    A 44-year-old male with severe hemophilia B was referred to our department because of nausea, vomiting, left lower limb hemiplegia, and left arm paresis.[ncbi.nlm.nih.gov] Steven Pipe, professor of pediatrics and pathology and pediatric medical director of the hemophilia and coagulation disorders program at the University of Michigan, had this[endpts.com] The Leyden phenotype of hemophilia B manifests as severe childhood disease, which subsequently improves at the onset of puberty, likely due to androgen effect.[emedicine.medscape.com]

  • HMG-CoA Lyase Deficiency

    Nausea and vomiting was attributed to hyperemesis gravidarum.[ncbi.nlm.nih.gov] J Pediatr. 2013 Jan 13. [Medline]. Berry GT, Steiner RD. Long-term management of patients with urea cycle disorders.[emedicine.medscape.com] Late diagnosis is associated with markedly advanced skeletal maturation and accelerated linear growth initially, but early natural puberty and ultimately short stature.[genico.ch]

  • Long Chain Hydroxyacyl-CoA Dehydrogenase Deficiency

    Long-chain 3-hydroxyacyl-coa dehydrogenase deficiency Long-chain 3-hydroxyacyl-coA dehydrogenase (LCHAD) deficiency is an inherited disease characterized by lethargy, weakness, vomiting[genetics.mytestingoptions.com] Hoffman Pediatric Cardiology (2009) Disorders of mitochondrial long-chain fatty acid oxidation R. J.[dx.doi.org] Late diagnosis is associated with markedly advanced skeletal maturation and accelerated linear growth initially, but early natural puberty and ultimately short stature.[genico.ch]

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