Gamuts

Kallmann syndrome

Kallmann syndrome (KS) is a genetic disorder that prevents a person from starting or fully completing puberty. Kallmann syndrome is a form of a group of conditions termed hypogonadotropic hypogonadism. [Source: Wikipedia ]

OrphaNet reference
Kallmann syndrome 
May Cause
Cleft lip/palate
Congenital renal or ureteral anomaly
Cryptorchidism
Deafness
Gynecomastia
Hypogonadism
Intracranial calcification
Microorchidism
Myopia
Neuronal migration disorder
Slipped capital femoral epiphysis
May Be Caused by
Brachytelephalangy - dysmorphism - Kallmann syndrome
Kallmann syndrome - heart disease
OrphaNet reference
Kallmann syndrome 
May Cause
Cleft lip/palate
Congenital renal or ureteral anomaly
Cryptorchidism
Deafness
Gynecomastia
Hypogonadism
Intracranial calcification
Microorchidism
Myopia
Neuronal migration disorder
Slipped capital femoral epiphysis
May Be Caused by
Brachytelephalangy - dysmorphism - Kallmann syndrome
Kallmann syndrome - heart disease


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