Neonatal Endocrinologic Problems in Collodion Babies

Ahmet Ozdemir1, Sabriye Korkut1, Selim Kurtoglu1,2

  • 1Division of Neonatology , Department of Pediatrics, Faculty of Medicine, Erciyes University, Kayseri, Turkey.

Insights

Collodion babies (CBs) often experience premature birth and small for gestational age (SGA) conditions. These infants show signs of growth hormone resistance, with higher GH and lower IGF-1/IGFBP-3 levels, alongside a notable increase in hypothyroidism.

Area of Science:

  • Endocrinology
  • Neonatology
  • Pediatric Growth Disorders

Background:

  • Collodion babies (CBs) present unique challenges in neonatal care.
  • Prematurity and small for gestational age (SGA) are common in CBs, necessitating investigation into associated endocrine issues.
  • Understanding growth-related endocrinopathies is crucial for the long-term health of CBs.

Purpose of the Study:

  • To investigate endocrinologic problems in collodion babies (CBs).
  • To specifically identify growth-related endocrine dysfunctions in newborns with collodion ichthyosis.
  • To compare growth hormone (GH), insulin-like growth factor 1 (IGF-1), and IGF binding protein-3 (IGFBP-3) levels with a control group.

Main Methods:

  • A study group of 42 clinically identified newborn collodion babies was recruited.
  • A control group was matched for gestational age and birthweight.
  • Serum samples were analyzed for thyroid function, GH, IGF-1, and IGFBP-3 levels.

Main Results:

  • Collodion babies exhibited lower IGF-1 and IGFBP-3 levels and higher GH levels compared to controls.
  • Ten CBs were diagnosed with primary hypothyroidism, 2 with subclinical hypothyroidism, and 1 with central hypothyroidism.
  • A significant difference in primary hypothyroidism prevalence was observed between groups (p=0.01).

Conclusions:

  • Collodion babies frequently experience premature birth and SGA.
  • Elevated GH and reduced IGF-1/IGFBP-3 levels suggest growth hormone resistance in CBs.
  • The increased incidence of hypothyroidism in collodion babies is a significant finding requiring attention.
Abstract

Related Concept Videos

Inborn Errors of Metabolism01:20

Inborn Errors of Metabolism

Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
970
Smooth Endoplasmic Reticulum01:21

Smooth Endoplasmic Reticulum

Smooth endoplasmic reticulum or smooth ER is a sub-organelle with specialized functions in animal cells and plant cells. It is often associated with the tubule morphology of the endoplasmic reticulum.
The ER provides optimal conditions for synthesizing steroid hormones and lipids, such as phospholipids and triglycerides. Traditionally, lipid metabolism was considered to be a smooth ER function. However, there is no direct evidence to prove that rough ER is completely excluded from lipid...
8.5K
Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
4.4K