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A genetic study of vitamin D deficiency rickets: 2-sex differences and ABO typing

M S el-Kholy1, F Y Abdel Mageed, F A Farid

  • 1Pediatric Department, Ain Shams Faculty of Medicine.

Insights

This study found a genetic link to vitamin D deficiency rickets, with a higher prevalence in males and association with Blood Group A. These factors suggest a genetic predisposition to nutritional rickets.

Area of Science:

  • Pediatrics
  • Genetics
  • Nutritional Science

Background:

  • Vitamin D deficiency rickets is a significant health concern in infants.
  • The role of genetic factors in the development of nutritional rickets requires further investigation.

Purpose of the Study:

  • To investigate potential genetic influences on vitamin D deficiency rickets.
  • To examine sex differences and ABO blood group associations in rachitic infants.

Main Methods:

  • A cohort of 400 infants diagnosed with rickets, aged 6 months to 2 years, was studied.
  • Data collected included sex, ABO blood typing, and alkaline phosphatase levels.

Main Results:

  • A statistically significant male predominance (sex ratio 1.43) was observed in rachitic infants (P < 0.001).
  • Blood group A showed a significant association with rickets in both sexes (P < 0.001).
  • Male infants exhibited significantly higher alkaline phosphatase levels (91% > 30 K.A. units) compared to females (72%), indicating greater disease severity.

Conclusions:

  • The findings support the hypothesis of a genetic component in nutritional rickets.
  • Sex and ABO blood group may be associated with susceptibility and severity of vitamin D deficiency rickets.

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