Kallmann Syndrome - causes, symptoms, treatment - review of literature [PDF]
Background: Kallmann syndrome is a rare congenital disorder characterized by hypogonadotropic hypogonadism and anosmia or hyposmia. KS results from abnormalities in the migration of GnRH neurons from the nasal placode to the hypothalamus.
Żak, Natalia
core +1 more source
Unilateral renal agenesis, blind-ended ureter, and ectopic ureterocele inserting into the seminal vesicle: A very rare developmental association. [PDF]
Sorour S, Ferguson C, Wilson MP, Low G.
europepmc +1 more source
Phalloplasty as a treatment for severe penile insufficiency [PDF]
Ceulemans, Peter +4 more
core +1 more source
Mirror Movements and Ichthyosis in a Child: A Rare Presentation of Kallmann Syndrome. [PDF]
Vachher H +3 more
europepmc +1 more source
A Novel Variant in <i>NR5A1</i> Resulting in Normosmic Hypogonadotropic Hypogonadism With Short Stature. [PDF]
Shah S +5 more
europepmc +1 more source
Management of Neonatal Isolated and Combined Growth Hormone Deficiency: Current Status [PDF]
Cerutti, Matteo +2 more
core +1 more source
Penile gangrene induced by colovesical fistula: a case report. [PDF]
Lu D +4 more
europepmc +1 more source
Phalloplasty in Children with Severe Penile Tissue Loss: Single Center Case Series. [PDF]
Demirtas G +6 more
europepmc +1 more source

