its sugary
This hormone is typically the first to rise in central precocious puberty.
LH!
This autosomal recessive disorder causes a musty body odor and intellectual disability if untreated.
PKU
This congenital heart defect is most commonly associated with Down syndrome.
AVSD
This virus is the most common cause of bronchiolitis in infants.
RSV
This seizure type is characterized by sudden loss of muscle tone and frequent falls.
Atonic seizure
This oral hypoglycemic agent is being studied for use in prediabetic adolescents
Metformin
This glycogen storage disease presents with hepatomegaly and fasting hypoglycemia.
Von gierkes disease
This heart sound is classically heard in patients with a patent ductus arteriosus.
Continuous machine murmur
This bacterial infection causes a pseudomembrane in the throat and is prevented by a vaccine
Diptheria
This condition presents with hypotonia, poor feeding, and a "floppy baby" appearance in infancy. whats the diagnosis
SMA
This genetic syndrome is associated with hypocalcemia due to parathyroid hypoplasia
Di george syndrome
This trinucleotide repeat disorder presents with macroorchidism and developmental delay.
Fragile x syndrome
This cyanotic heart defect is characterized by right ventricular outflow tract obstruction and a boot-shaped heart.
TOF
This congenital infection presents with periventricular calcifications and sensorineural hearing loss.
Rubella
This reflex disappears by 4–6 months
moro reflex
This test is used to differentiate between central and nephrogenic diabetes insipidus
water deprivation test
This enzyme is deficient in classic galactosemia.
galactose-1-phosphate uridyltransferase
This arrhythmia is most common in neonates and often treated with adenosine.
SVT
This disease presents with a "slapped cheek" rash. name the disease
Erythema infectiosum
This is the most common cause of status epilepticus in children.
febrile seizure
his condition is characterized by tall stature, delayed puberty, and small testes in boys
This syndrome is caused by a deletion on the paternal chromosome 15q11-q13.
Prader willi syndrome
This pulse finding is associated with coarctation of the aorta.
Radiofemoral delay
This is the first-line antibiotic for treating acute otitis media in children.
Amoxicillin
This neurocutaneous syndrome is associated with café-au-lait spots and optic gliomas.
NF1