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PedAM

Pediatric Disease Annotations & Medicines




Disease n syndrome
Phenotype C0034012|delayed puberty
Sentences 2
PubMedID- 20543690 Recent findings: substantial variation in clinical expression, from complete anosmia and hypogonadotropic hypogonadism to delayed puberty and normosmia, of the same kallmann syndrome gene defects including in newer ones (fgf8 and chd7) continues to be repeatedly observed.
PubMedID- 24189182 Loss-of-function mutations of kal1 results in kallmann syndrome with delayed puberty and anosmia.

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