normal male,external genitalia
LH/FSH
increased
LH/FSH
Iow basal/after GnRH
Yes
Anorchidism/ cryptorchism |
No |
Testes present | |
Yes | |||
Primary |
1 |
r | |
testicular |
Yes | ||
insufficiency due |
◄- |
General illnesses | |
to generał | |||
illness |
No |
Primary testicular nsufficiency after exposure to toxins
Yes
Orchiditis, trauma, radiotherapy, exposure to toxins
Yes
Normal |
No |
Kallmanns- | |
olfactory sense |
syndrome | ||
1 |
Yes | ||
Secondary | |||
General illnesses, |
Yes |
hypogonadism | |
underweight |
-► |
with generał | |
illness, • | |||
anorexia | |||
1 |
No r | ||
Clinical | |||
signs of |
Yes |
Cushing s | |
hyper- |
-► |
disease |
No
Yes
No
No r | |
Autoimmune diseases | |
No | |
Małe karyotype 46,XY | |
' |
Yes r |
No
Further
endocrine
deficits
Yes
No
Familial factor with delayed pu berty, spontaneous onset of puberty after therapy with testosterone
45,X0/46,XY and variants
Encephalitis, meningitis, trauma, Radiotherapy, cranial pressure, detection of tumor on CT/MRI
No
Yes
Clinical signs ofTurners syndrome
' |
' |
Yes |
Klinefelters
syndrome
Noonan
syndrome
CNS lesion or CNS tumor
Idiopathic hypogonado-tropic hypo-gonadism
Constitutional
delayed
development
Figurę 2.4: Explanation of delayed puberty in a boy.