WEDNESDAY, June 21, 2023 (HealthDay News) -- When people think about Alzheimer's disease, they usually associate it with seniors who have had a long and fulfilling life.
Sadly, two rare conditions that imitate the symptoms of Alzheimer's strike infants and children. Two of these disorders, Niemann-Pick Disease Type C (NPC) and Sanfilippo syndrome, will be discussed here. Here is everything you need to know about childhood Alzheimer’s, including what it is, its causes and risk factors, symptoms and treatments.
What is childhood Alzheimer's?
Sanfilippo syndrome and NPC cause symptoms resembling dementia, hence the reference to childhood Alzheimer’s disease. These diseases are lysosomal storage disorders. The Cleveland Clinic states that people with a lysosomal storage disorder lack certain enzymes that help the body break down fats, sugars and other substances. These substances cannot be properly stored by the body and then cause harm when they build up in the body.
Childhood Alzheimer's causes and risk factors
Boston Children’s Hospital advises that a genetic mutation in the NPC1 or NPC2 gene causes NPC. The disease is inherited in an autosomal recessive pattern, which means that to be affected, the child must receive a defective gene copy from each parent. NPC results in an abnormal storage pattern of fat molecules inside cells.
Sanfilippo syndrome is also a genetic disorder that is inherited in an autosomal recessive pattern, with a defective gene from each parent. Sanfilippo disease results in an inability to break down heparan sulfate, which then builds up in the body, causing harm.
Childhood Alzheimer's symptoms
Because Sanfilippo syndrome and NPC are different diseases, their symptoms differ.
NPC symptoms typically begin in childhood, although they can present at any time, including adulthood.
According to Boston Children’s Hospital, symptoms include:
Difficulty coordinating movement
Abnormal eye movement
Poor muscle tone
Severe liver disease
Frequent respiratory infections
Difficulty with speech
Loss of cognitive skills
Difficulty with swallowing and feeding
Children with Sanfilippo syndrome typically appear healthy at birth and do not tend to show symptoms right away; some of the early signs are typical of common childhood conditions. The Cure Sanfilippo Foundation lists the following symptoms:
Transient tachypnea of the newborn (fast breathing after birth)
Coarse facial features (prominent forehead, full lips and nose)
Excessive body hair
Large head size
Speech and development delays
Recurring ear/sinus infections
Chronic upper respiratory congestion
Features of autism
Diarrhea, loose stools
Continued coarsening of facial features
Development of features of autism
Brain atrophy (shrinking of brain tissues)
Loss of ambulation
Loss of oral feeding
Childhood Alzheimer’s treatment
There is currently no cure for either Sanfilippo syndrome or NPC. Treatment for both of these diseases is supportive. Treatment at a dedicated multidisciplinary center is ideal for helping manage specific symptoms of each condition. Endocrinologist Venkatraman Rajkumar says in StatPearls, “It helps prevent delays, decreases patients lost to follow-up and vastly improves outcomes.”
Living with childhood Alzheimer’s
Is childhood Alzheimer's terminal? Life expectancy with a diagnosis of Sanfilippo syndrome is 10 to 20 years of age. Life expectancy with NPC varies greatly, depending on the severity of the disease. Often receiving the correct diagnosis is difficult because while childhood Alzheimer’s life expectancy is limited, it can mimic common childhood illnesses.
Kidshealth.org has helpful advice for when you have received a life-changing diagnosis for your child:
Surround your child and your family with loving support
Seek therapy when needed to help cope with both the child's and the parents' feelings
Educate yourself and your child as much as possible; as a parent, you will be your child’s best advocate