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10 Possible Causes for Delayed Growth and Development, Night Blindness, Thyroid Binding Globulin Decreased

  • Myxedema

    Poor growth, resulting in short stature Delayed development of permanent teeth Delayed puberty Poor mental development When to see a doctor See your doctor if you're feeling[mayoclinic.org] Hypothyroidism in children and teens In general, children and teens who develop hypothyroidism have the same signs and symptoms as adults do, but they may also experience:[mayoclinic.org]

  • Malabsorption Syndrome

    […] over time as a result of chronic malabsorption: Anemia Delayed growth and development in children Difficulty concentrating, confusion, and sometimes personality changes Malnutrition[labtestsonline.org] Impaired absorption of vitamin A could result in poor vision and night blindness as well as dermatitis.[web.archive.org] Inflammation of mouth (stomatitis) Easy bruising, bleeding gums Numbness and tingling in feet and hands Paleness Muscle or bone pain The following are some complications that can develop[labtestsonline.org]

  • Celiac Disease

    These cases consisted of subjects presenting with various GIS symptoms and indicated for endoscopy (with chronic diarrhea, delayed growth and development, abdominal pains,[ncbi.nlm.nih.gov] […] folate deficiency) Growth failure in children Bone pain (osteoporosis and osteopenia, vitamin D and calcium deficiency) Muscle cramps (magnesium and calcium deficiency) Night[ojrd.com] In children, untreated celiac disease can cause stunted growth, delayed development and behavioral issues. For women, untreated celiac disease can lead to infertility.[livescience.com]

  • Juvenile Myxedema

    Childhood (juvenile) hypothyroidism is characterized by delayed growth and problems with mental development; however, with prompt treatment, problems can be minimized.[medbroadcast.com] Conversely, androgens and corticosteroids may decrease serum concentrations of Levothyroxine-binding globulins.[medicines.org.uk] blindness 264.6 With xerophthalmic scars of cornea 264.7 Other ocular manifestations of vitamin A deficiency Xerophthalmia due to vitamin A deficiency 264.8 Other manifestations[theodora.com]

  • 48,XXYY Syndrome

    Common physical features may include tall stature, reduced muscle tone, small testes (hypogonadism), delayed pubertal development and lack of secondary male sex characteristics[rarediseases.org] Although clinical hypothyroidism is rare, decreased 131 I uptake and poor responsiveness to thyroid-stimulating hormone have been reported. 53, 54 Thyroid-binding globulin[glowm.com] Karampelas et al. described an adult with a high myopia and night blindness.[omicsonline.org]

  • Radioulnar Synostosis-Microcephaly-Scoliosis Syndrome

    […] speech and language development Macrocephaly Autosomal dominant inheritance Ataxia Abnormal facial shape Hirsutism Wide mouth Thick vermilion border Intrauterine growth retardation[mendelian.co] Although clinical hypothyroidism is rare, decreased 131 I uptake and poor responsiveness to thyroid-stimulating hormone have been reported. 53, 54 Thyroid-binding globulin[glowm.com] Night blindness skeletal anomalies unusual facies 0 *Myopia *Night Blindness *Facies.[reference.md]

  • Lower Limb Deficiency-Hypospadias Syndrome

    growth and development.[ts4jc.wordpress.com] […] of rod cells (night blindness/periopheral vision loss) then cone cells/macula (central acuity loss) Connective tissue disorder, related with Marshall syndrome AD inheritance[quizlet.com] Although clinical hypothyroidism is rare, decreased 131 I uptake and poor responsiveness to thyroid-stimulating hormone have been reported. 53, 54 Thyroid-binding globulin[glowm.com]

  • Thyro-Cerebro-Renal Syndrome

    Development (cognitive, Motor, Language, Social-Emotional) Plan for delays, especially in language development.[medicalhomeportal.org] Decreased levels of total T4 and total T3 are also the result of decreased thyroid hormone binding proteins (thyroxine binding globulin [TBG], transthyretin, and albumin).[cancertherapyadvisor.com] Progressive degeneration of the retina that can advance to near-blindness Night blindness is an early and prominent symptom Atypical retinitis pigmentosa The macula may or[tsbvi.edu]

  • Autosomal Dominant Dyskeratosis Congenita 2

    General physical and mental development is sometimes delayed, and osteoporosis may occur.[idoj.in] In addition, other treatment-related findings detected were a significant decrease in thyroid binding globulin, accelerated growth in prepubertal children, and splenic peliosis[dovepress.com] Blindness, Congenital Stationary, Type 1A 3 Night Blindness, Congenital Stationary, Type 1B 2 Night Blindness, Congenital Stationary, Type 1C 2 Night Blindness, Congenital[preventiongenetics.com]

  • Autosomal Recessive Dyskeratosis Congenita Type 5

    General physical and mental development is sometimes delayed, and osteoporosis may occur.[idoj.in] In addition, other treatment-related findings detected were a significant decrease in thyroid binding globulin, accelerated growth in prepubertal children, and splenic peliosis[dovepress.com] Blindness, Congenital Stationary, Type 1A 3 Night Blindness, Congenital Stationary, Type 1B 2 Night Blindness, Congenital Stationary, Type 1C 2 Night Blindness, Congenital[preventiongenetics.com]

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