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  • 46,XX disorder of sex development associated with skin abnormalities due to homozygous R-Spondin 1 loss of function mutation

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Case Reports: Rare disease
46,XX disorder of sex development associated with skin abnormalities due to homozygous R-Spondin 1 loss of function mutation

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Cite this article as:
Divyasri N, Varma P, Kunnuru S, et al
46,XX disorder of sex development associated with skin abnormalities due to homozygous R-Spondin 1 loss of function mutation
BMJ Case Reports CP 2024;17:e255466.