Rare Hybrid Baby, Defying Odds Amidst Heteroditary Skin Disorder, Affected Vision, and Hearing.

Recently, Quang Ninh Obstetrics and Gynecology hospital reported a 27-year-old mother, who gave birth at 32 weeks prematurely. The baby was born with an abnormality of dry skin all over the body and was diagnosed with the disease. Harlequin Ichthyosis, an inherited skin disorder. It is known that the mother gave birth for the 6th time, did not go to the doctor and monitor the pregnancy, did not perform prenatal screening tests. However, the baby's whole body skin is hard and thick, accompanied by deep cracks that cause burning pain.

Dr. Dang Hong Duypen, Department of Neonatology, Quang Ninh Obstetrics and Gynecology Hospital, said that Harlequin Ichthyosis is an extremely rare and severe genetic disorder characterized by dry skin with fish-like scales, belonging to a group of recessive genetic diseases with an incidence of about 1 in 500,000. The disease makes the dermis 10 times thicker than normal and the skin growth rate 7 times faster than in normal people.


Image: Having a genetic skin disorder, an infant has dry skin all over the body - Photo 1.

Children with rare skin diseases

The genetic skin disorder Harlequin Ichthyosis in a simple way is that in the evolutionary process of our ancestors, to switch from the water environment in the mother's uterus to the dry environment after birth, the body Humans have formed a self-protective mechanism of the skin called keratinization, the technical term is Keratinization.

The cause of the disease is a mutation in the recessive gene on chromosome 2, the ABCA12 gene (2595 amino acids) that regulates the synthesis of ABCA12 protein (ATP-binding cassette transporter 12) in the skin – a protein responsible for transporting lipids to the epidermis. Creates a protective barrier for the skin. Lack or absence of ABCA12 protein in the skin layer, causing lipids not to be transported out but deposited in the cell membrane, making the stratum corneum thicker and harder.

The type of mutation is recessive on the autosomal chromosome, so the child "inherits" both the mutated gene from both parents.

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