Menkesdisease,alsoknownaskinkyhairsyndromeorcopperdeficiencydisorder,isanautosomalrecessivegeneticconditioncharacterizedbysevere铜代谢紊乱andassociatedwithvariousneurologicalsymptomssuchasdevelopmentaldelay,seizures,andmuscleweakness.

ThediseaseiscausedbymutationsintheATP7Agene,whichcodesforaproteininvolvedincoppertransportandmetabolismwithincells.Copperdeficiencyleadstodisruptionofcellularfunctions,includingneuronaldevelopmentandfunction,resultingintheclinicalmanifestationsdescribedabove.
DiagnosisofMenkesdiseasetypicallyinvolvesbloodtestsmeasuringcopperlevels,urinarycopperexcretion,andgenetictestingformutationsintheATP7Agene.
Treatmentconsistsofdietarysupplementationwithcopper,oftenthroughoralchelationtherapyusingpenicillamine.Earlydiagnosisandinterventioncanimproveoutcomesforaffectedindividuals.

Overall,Menkesdiseaseisararebutseriousgeneticconditionthatrequiresspecializedcareandmanagement.