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Dental Hyper Pigmented Disorders 1c223fae

Mode of inheritance of incontinentia pigmenti is:

A
Autosomal dominant
B
Autosomal recessive
C
X linked dominant
D
X linked recessive
High-Yield Explanation
Incontinentia pigmenti - X-linked dominant Developmental defects of eye, teeth, CNS with cutaneous lesions. Four clinical stages - Inflammatory macules, papules, vesicle. Hyperkeratotic & verrucous lessions Grey-brown pigmentation Atrophic, hypopigmented & depimented - Initially hyperpigmented lesions ; as it progresses towards 4th stage , it becomes hypopigmented - Lesions follow the lines of blaschko. X linked dominant diseases-Vit- D resistant rickets (X linked hypophosphataemia)-Rett syndrome-Incontinentia pigmenti-Alpo syndrome-Fragile X syndrome-Goltz syndrome-X linked protoporphyria

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