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1,818 Possible Causes for Delayed Bone Age, Hypophosphatemia, Supraclavicular Fat Pads

  • Iatrogenic Cushing's Disease

    The indica ted treatment was topical with hydrocortisone acetate and delayed bone age (BA) (6 months BA for 1 year 3 months in chronological age).[] Common: centripetal obesity with dorsocervical and supraclavicular fat pads, facial plethora and "moon face," fatigue, hyperglycemia, hypertension, mood lability, easy bruisability[] Individuals with Cushing syndrome can develop moon facies, facial plethora, supraclavicular fat pads, buffalo hump, truncal obesity, and purple striae, as shown in the image[]

  • Cushing's Disease

    Individuals with Cushing syndrome can develop moon facies, facial plethora, supraclavicular fat pads, buffalo hump, truncal obesity, and purple striae, as shown in the image[] fat pads (buffalo hump) Usually, very slender distal extremities and fingers Muscle wasting and weakness are present.[] At baseline and at months 6 and 12, a reviewer at each site assessed patients for signs of hypercortisolism (facial rubor and supraclavicular and dorsal fat pads) by scoring[]

  • Vitamin D Deficiency

    The current patient presented with distal RTA, hypocalcemia, and hypophosphatemia that were found to be secondary to both vitamin D deficiency and pSS.[] She presented with fractures during the first year-of-life followed by bone deformities, delayed development, failure-to-thrive, and pneumonias.[] In this paper, we report two cases showing the deleterious consequences of vitamin D deficiency in HD patients which is characterised by hypophosphatemia, hypocalcemia and[]

    Missing: Supraclavicular Fat Pads
  • Adrenal Cortex Hormone

    The adrenal cortex secretes steroid hormones. In this lesson, you will learn about two of these steroid hormones: glucocorticoids, which help you deal with long-term stress, and androgens, which influence male sexual characteristics. Adrenal Cortex Adrenal glands are located on top of the kidneys. The adrenal glands[…][]

  • Celiac Disease

    The patient had normal anion-gap metabolic acidosis (pH   7.16) with persisting hypokalemia, hyponatremia, hypomagnesemia and hypophosphatemia.[] […] density Unexplained infertility Delayed puberty, late menarche/early menopause Unexplained miscarriage, premature birth, or small for gestational age infant Dental enamel[] […] migraine Dermatological manifestations (such as rash, psoriasis, blisters) Peripheral neuropathy Unexplained chronic hypertransaminasemia [ 57 ] Folic acid deficiency Reduced bone[]

    Missing: Supraclavicular Fat Pads
  • Anterior Pituitary Hypofunction

    […] magnesium intake Lithium use Causes of Decreased Excessive Urinary Losses Renal dysfunction (Tubular acidosis, glomerulonephritis, interstitial nephritis, etc) Hypercalcemia or hypophosphatemia[] : delayed fusion of epiphyses; bone growth does not match the age of the child - adults have hypoglycemia: decreased gluconeogenesis; loss of muscle mass; increased adipose[] - in Hypopituitarism, neither ACTH or 11-deoxycortisol are increased 2) GROWTH H'MONE (GH): - decreased GH decreases synthesis & release of IGF-1 - children have growth delay[]

    Missing: Supraclavicular Fat Pads
  • Childhood Celiac Disease

    Additional findings included short stature, delayed bone age, and impaired xylose absorption.[]

    Missing: Supraclavicular Fat Pads
  • Cooley's Anemia

    This type can cause symptoms of moderate to severe anemia including: Extreme tiredness (fatigue) Pale skin Slow or delayed growth Weak bones Enlarged spleen Beta thalassemia[] The diagnosis is most often made between ages 6 and 12.[]

    Missing: Supraclavicular Fat Pads
  • X-Linked Hypophosphatemia

    X-linked hypophosphatemia (XLH) is the most common form of familial hypophosphatemia.[] Hypophosphatemia 00754 at CHORUSHypophosphatemic rickets; XLH; Hypophosphatemia, vitamin D-resistant rickets at NIH's Office of Rare Diseases The PHEXdb - a database of nucleotide[] Abstract X-Linked hypophosphatemia (XLH) is the most common form of hereditary rickets caused by loss-of function mutations in the PHEX gene.[]

    Missing: Supraclavicular Fat Pads
  • Adrenocortical Carcinoma

    pads.[] The majority of patients with functional tumors shows symptoms of Cushing syndrome including truncal obesity, striae, malar flushing, supraclavicular and dorsocervical fat[]

    Missing: Delayed Bone Age

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