Unit Code 88540:
Kallmann Syndrome, Xp22.3 Deletion, FISH
Useful For
Aiding in the diagnosis of Kallmann syndrome, in conjunction
with conventional chromosome studies (#8696 "Chromosome
Analysis, for Congenital Disorders, Blood")
Detecting cryptic translocations involving Xp22.3 that are not
demonstrated by conventional chromosome studies
Special Instructions and Forms
Method Name
Fluorescence In Situ Hybridization (FISH)
Reporting Name
Kallmann, Xp22.3, FISH
Ordering Mnemonic
FKAL
Aliases
FISH
FISH (Fluorescent In Situ Hybridization)
Kallman Syndrome
Kallmann Syndrome
Kalman Syndrome
Xp Deletion
Xp22.3
External
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Excel
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