Acromegaly results from overproduction of growth hormone in adults, causing enlargement of bones and soft tissue in the face, hands, feet, and other parts of the body.
Acromegaly
Secretes too much growth hormone, in adulthood from an adenoma on pituitary
Acromegaly signs/symptoms
Bony/soft, insidious/progressive/slow onset, excessive growth of hands, feet, jaw and internal organs
Gigantism
Secretes too much growth hormone, before growth plates are fused/closure of epiphyses
Infant hypoglycemia/micropenis, delayed puberty, adults have dec bone density/muscle mass, long bone growth is slowed, causes poorly developed sexual organs, impaired sexual maturation, skeletal deformities/kyphosis, sleep apnea, spinal stenosis, motor delays, hearing infections/loss
Pituitary dwarfism diagnosis
2.5 deviations below normal mean
Pituitary dwarfism lab findings
Low GH, low IGF1, bone age is two yrs behind, CT/MRI of brain
Dwarfism
Autosomal dominant, variant in GFRG3, 80% new mutations, 20% inherited, if both parents have achondroplasia, 25% lethal risk
Dwarfism clinical features
Short/disproportionate, long bones short, macrocephaly, delayed motor development, cognitive development is normal, Rhizomelic shortening, bradydactyly, kyphosis, lordosis, saddle nose deformity, knee deformities, cervicomedullary compression
Dwarfism complications
OM, obs sleep apnea, obesity, leg bowing, spinal stenosis, cervical medullary compression