Prolonged neonatal jaundice

Neonatal jaundice refers to a yellowing of the skin and other tissues of a newborn infant as a result of increased concentrations of bilirubin in the blood. Neonatal jaundice affects over half of all newborns to some extent in the first week of life. Prolonged neonatal jaundice is said to be present if the jaundice persists for longer than 14 days in term infants and 21 days in preterm infants.

Also called: Neonatal jaundice, Prolonged yellowing of skin in newborn, Jaundice, neonatal.

Not sure what prolonged neonatal jaundice might be related to? See the lab tests that healthcare providers may use to investigate prolonged neonatal jaundice, and the conditions they help explore.
Explore relevant lab tests
Associations

Conditions associated with prolonged neonatal jaundice

The following conditions have been associated with prolonged neonatal jaundice in medical literature. This is informational and not a diagnosis.

Aicardi-Goutières syndrome

Aicardi-Goutières syndrome is a medical condition that may be associated with various symptoms and signs....

General

Athyreosis

Athyreosis is a medical condition that may be associated with various symptoms and signs....

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Hardikar syndrome

Hardikar syndrome is a medical condition that may be associated with various symptoms and signs....

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Houge-Janssens syndrome 4

Houge-Janssens syndrome 4 is a medical condition that may be associated with various symptoms and signs....

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Isolated thyroid-stimulating hormone deficiency

Isolated thyroid-stimulating hormone deficiency is a medical condition that may be associated with various sym...

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Melnick-Needles syndrome

A otopalatodigital syndrome spectrum disorder and is associated with a short stature, facial dysmorphism, osse...

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Menkes disease

Menkes disease is a medical condition that may be associated with various symptoms and signs....

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Sotos syndrome

Sotos syndrome is a medical condition that may be associated with various symptoms and signs....

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Sotos syndrome

Sotos syndrome is a rare multisystemic genetic disorder characterized by a typical facial appearance, overgrow...

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biliary, renal, neurologic, and skeletal syndrome

biliary, renal, neurologic, and skeletal syndrome is a medical condition that may be associated with various s...

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cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1

cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1 is a medical c...

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choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome

Choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome is an autosomal dominant disorde...

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developmental and epileptic encephalopathy 118

developmental and epileptic encephalopathy 118 is a medical condition that may be associated with various symp...

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microcephalic osteodysplastic primordial dwarfism type I

A microcephalic osteodysplastic primordial dwarfism that has material basis in homozygous or compound heterozy...

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mitochondrial DNA depletion syndrome 6 (hepatocerebral type)

mitochondrial DNA depletion syndrome 6 (hepatocerebral type) is a medical condition that may be associated wit...

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neurodevelopmental disorder with variable familial hypercholanemia

neurodevelopmental disorder with variable familial hypercholanemia is a medical condition that may be associat...

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neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2

neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2 is a medical condition that may ...

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osteootohepatoenteric syndrome

osteootohepatoenteric syndrome is a medical condition that may be associated with various symptoms and signs....

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peroxisome biogenesis disorder 1A (Zellweger)

peroxisome biogenesis disorder 1A (Zellweger) is a medical condition that may be associated with various sympt...

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triosephosphate isomerase deficiency

Triosephosphate isomerase (TPI) deficiency is a severe autosomal recessive inherited multisystem disorder of g...

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Tests

Tests providers may use to investigate prolonged neonatal jaundice

When investigating prolonged neonatal jaundice, a healthcare provider may order one or more of the following laboratory tests. Test selection is a clinical decision made by a qualified professional.

CBC with Differential

Measures red blood cells, white blood cells, and platelets to help evaluate overall health and detect disorder...

Sample: Blood

Comprehensive Metabolic Panel (CMP)

Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar ...

Sample: Blood

Ferritin

Measures iron stores in the body....

Sample: Blood

Folate

Measures folate levels to help evaluate anemia and pregnancy health....

Sample: Blood

Free T4

Measures the active form of thyroxine to help evaluate thyroid function....

Sample: Blood

Iron Panel

Measures iron, TIBC, transferrin saturation, and ferritin....

Sample: Blood

Thyroid Stimulating Hormone (TSH)

Screens for thyroid disorders such as hypothyroidism and hyperthyroidism....

Sample: Blood

Uric Acid

Helps diagnose and monitor gout and kidney stones....

Sample: Blood

Urinalysis

Examines urine content to help detect urinary tract infections, kidney disease, and diabetes....

Sample: Urine

Vitamin B12

Detects B12 deficiency which can cause anemia and neurological symptoms....

Sample: Blood

Related

Symptoms commonly seen alongside prolonged neonatal jaundice

When to seek care

Seek care from a qualified healthcare provider if prolonged neonatal jaundice is severe, persistent, worsening, or accompanied by concerning symptoms. If you think you have a medical emergency, call your local emergency number immediately.

FAQ

Frequently Asked Questions

What does the symptom prolonged neonatal jaundice mean?

Prolonged neonatal jaundice is a health sign or symptom described in medical literature. Neonatal jaundice refers to a yellowing of the skin and other tissues of a newborn infant as a result of increased concentrations of bilirubin in the blood. Neonatal jaundice affects over half of all newborns to some extent in the first week of life. Prolonged neonatal jaundice is said to be present if the jaundice persists for longer than 14 days in term infants and 21 days in preterm infants.

Which conditions are associated with prolonged neonatal jaundice?

Prolonged neonatal jaundice has been reported in association with 20 conditions in the medical literature we index, including Aicardi-Goutières syndrome, Athyreosis, Hardikar syndrome, Houge-Janssens syndrome 4, Isolated thyroid-stimulating hormone deficiency. These associations do not mean you have any of these conditions.

Should I see a doctor about prolonged neonatal jaundice?

You should discuss any persistent or concerning symptoms with a qualified healthcare provider. This website does not provide diagnosis. If you have severe symptoms or signs of a medical emergency, seek care immediately.

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