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Unit Code 88540:
Kallmann Syndrome, Xp22.3 Deletion, FISH

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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


Key