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Raising Christopher

LCHAD deficiency has robbed children of their sight, then their lives, but Emory researchers are out to change that.

By Rhonda Mullen, Photography by Jack Kearse

Christopher Harry likes to play baseball, read books with his parents, and play drums with his dad. But living with a rare metabolic disorder makes this ordinary 4-year-old extraordinary. Jack Kearse

Watching Christopher Harry whack a baseball with a bright orange, plastic bat or hearing him pound a syncopated beat on a small drum, you'd never guess that the energetic 4-year-old has a rare metabolic disorder.

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency may be too big a mouthful for Christopher to pronounce, but he knows what LCHAD means. It means his body is special. It means he can have only a few grams of fat a day. It means he needs to eat often, every two hours or so, to give his body enough energy to grow.

Christopher was the first baby born in Georgia to be identified with LCHAD deficiency through newborn screening soon after the disorder was added to the newborn screening panel in the state. His mother, Stephanie Harry, almost died when she developed a potentially fatal complication late in her pregnancy. The condition sometimes occurs when the mother is carrying a baby with a fatty acid oxidation disorder (FAOD). Doctors suspect that Stephanie's liver and kidneys may have been trying to compensate for what Christopher's body was unable to process.

Since then, Harry has steeped herself in learning about her son's disorder and how to keep him healthy. She now knows that LCHAD deficiency is a rare inherited FAOD in which the body is unable to break down certain fats to use for energy. She knows that it is so rare—both parents have to carry the recessive gene—and so little understood that many people don't recognize it, even clinicians, who may go an entire career without seeing a single case. She knows that babies who were previously thought to have died of SIDS or liver or kidney failure may actually have had LCHAD.

Harry also knows that when most people exercise or get sick, they use the long-chain fats stored in their body or found in most food for energy. But when Christopher gets sick, he is unable to use this fat for energy. When unable to consume food or medical formula, his body runs out of glucose and starts breaking down muscle, producing by-products that can be toxic. These toxic by-products can affect many systems in the body, in particular the kidneys and heart, leading to serious complications.

This past January, Christopher had his first hospitalization when his blood levels of creatine kinase (CK)—a biomarker used to confirm damage to muscles—shot up to 70,000. By comparison, a marathoner at a race's finish might have a CK level of 11,000, which recovers to normal after rest.

Maybe scariest of all for Stephanie Harry and her husband Ryan, a kindergarten teacher, is the unknown future. Christopher started preschool this fall, and they have to get him through school with the usual exposure to germs that all children face but without the usual resiliency and metabolism that most kids have. And they have to do what they can to keep their blue-eyed boy from losing his sight. Children with the deficiency have a high chance of developing pigmentary retinopathy, which can lead to blindness.

The Harrys, however, are not without help or hope. As soon as Christopher's newborn screening test showed an abnormality, the Emory Metabolic Genetics Nutrition Program has been there for the family. The only program in Georgia to offer complete services for managing metabolic disorders, the clinic follows up on 5,000 abnormal newborn screening tests each year by analyzing biomarkers in blood and urine and confirming a diagnosis. The clinic's geneticists and nutritionists treat some 250 children with metabolic disorders annually while genetic counselors work closely with their families.

Rani Singh

A mother herself, Rani Singh directs the genetic nutrition program at Emory, managing children with a range of metabolic disorders locally and working to standardize care for metabolic disorders nationally.

Stephanie Harry remembers the first day they met Rani Singh, the clinic's director of genetic nutrition. Christopher was six weeks old and had been discharged from the hospital only two days before. Harry herself was still recovering from liver failure and had a yellow tinge to her skin. "Ryan and I sat down with a woman who had so much warmth and concern for our family," she says. "The news of our son's diagnosis was hard, but after meeting with Dr. Singh and her staff, I felt comforted and blessed that we had such amazing people walking alongside us through unfamiliar territory. We were so vulnerable, but the staff took the necessary time to answer every question that arose that day and in the months to come."

Connecting research to families 

It is families like the Harrys who keep Singh in the clinic, she says. A registered dietitian with a PhD in nutrition, she is actively involved in research to learn more about the 22 known primary metabolic disorders and another 30 related secondary conditions recommended for screening by the American College of Medical Genetics. She is seeking to standardize care in the country, setting up databases for both clinicians and families, advocating for her patients, and arguing for an educational specialty track for advanced practice nutritionists.

Her job can be stressful as the lead dietitian in Emory's clinic. On a recent day, Singh was on deadline for completing a grant application, on the phone to convince an insurance company to cover the costs of a nutrition intervention for a new patient, and closely monitoring the nutritional aspects of another patient who had experienced a sudden drop in heart rate. But despite the pressure that a busy clinical practice adds to her research load, Singh says she wouldn't want to pursue research in isolation.

"It is the connection with patients that makes it feel real," she says. "I look at someone like Christopher, and I know I can't quit patient care."

Singh currently manages six children with LCHAD deficiency. She attributes much of what she's learned about the little-understood disorder to one patient in particular, a young girl who had practically lived in the hospital until Singh entered the picture. The dietitian developed a diet of medium-chain fats for the 8-year-old, resulting in a dramatic decrease in the girl's number of hospitalizations. She saw her patient grow from a child to a young adult, watching as the girl lost first her vision, then use of her legs, and ultimately her life. "She taught me a lot," Singh says.

Children like Christopher Harry have benefited from Singh's experience with her first LCHAD patient. She arranged an overnight shipment of a just-released medical formula from manufacturers in the United Kingdom to Christopher's bedside so that he has been treated since birth. The formula includes a delicate balance of different kinds of fat and fat grams, not enough to overwhelm Christopher's body but enough for brain and eye development. One of its main ingredients, MCT oil, is found naturally in coconut.

Coverage for medical food varies by insurance companies and sometimes even month by month from the same carrier, as the Harrys have experienced. The Medical Foods Coalition of Georgia was formed with the sole mission to get insurance companies in the state to cover special medical food for children and adults with certain conditions. See for more information.

The Harrys have become experts in counting fats, which occur even in fruits and vegetables. Coconut oil is a staple in their kitchen, and they even made cookies with it last Christmas. As a baby, Christopher could have no more than 2 grams of fat each day. Now that he's grown, he can have up to 6. He needs to eat about every two hours because his body constantly uses up the incoming sugar, protein, and medium-chain fats. He calls the formula that he drinks his Power Moo.

"We've had to relearn how to cook," says his mom. In her kitchen, she keeps a brown envelope filled with modified recipes that work for the family: steamed vegetables, chicken with a rub rather than a marinade, and pancakes (Christopher's current favorite.)

But the manufactured medical formula, the Power Moo, is what sustains children with LCHAD deficiency. Because the formula is a food rather than a drug, insurance coverage varies by companies and even by month from the same carrier, as the Harrys have experienced. Yet it should be covered, says Singh. "Medical foods—what we call the specialized formulas for rare disorders—are life-saving treatments, and their cost can be high. Plus they have to be given for life," she says. Singh says that it is painful to watch families struggle to buy the formula without insurance help. "We screen every baby as a public health program, but we don't have a program to provide the means to treat every baby. These families fall through the cracks."


Each year, Emory hosts a summer camp for children ages 12 and up with metabolic disorders. This year, a former camper returned to lead the sessions. Born with the most publicized of all metabolic disorders, phenylketonuria or PKU, the girl was off her prescribed diet when she first attended camp. Today she's getting a master's degree in nutrition.

Singh beams with pride when she tells the story. "It's hard for me not to get bonded with my patients," she says. How could she not? She is alongside them as they grow up. She is touched by their bravery and their struggles. She sometimes sees them die.

This involvement fuels her drive to learn more. One fundamental LCHAD research question is whether children placed on the premixed formula from birth, like Christopher, will be able to retain their sight. So far, patients who began taking the formula as older children have lost their sight eventually.

"We don't understand loss of vision," Singh says. "One theory posits that it occurs from toxic buildup that causes changes in the eye. Another group believes that it has something to do with the essential fatty acids—omega 3 and omega 6—not being utilized. To me, the symptoms seem like a vitamin E deficiency."

Because so much is still to be discovered, tried, and verified, treatment for FAODs varies widely across the country. Singh is trying to change that—to collect evidence and enable practitioners to reach a consensus that will lead to standardized care. As the principal investigator on a federal Health Resources and Services Administration grant, she is collaborating with seven regional groups to build a research base for FAODs. In June, a new patient registry was launched, where families affected by a FAOD will be able to voluntarily submit their own information, share recipes, and learn about clinical trials.

"We are empowering them by helping them know what to expect," Singh says. "We're building an infrastructure together."

Singh also would like to see a track for advanced genetics and nutrition management, a profession she says that saves lives but sometimes lacks the recognition that it deserves. For example, she remembers a case when she worked with a cardiac surgeon on a treatment for a patient who had an FAOD. The child was scheduled for a heart transplant, but Singh convinced the doctor and the parents to let her intervene with nutrition treatment. She did so, and the boy's heart normalized. He no longer needed a transplant and has since been able to attend school with his friends. "I don't need a randomized trial to tell you that nutrition management works in these patients," Singh says.

My Special Body

Speaking out

The Harrys know that. They live it every day.

By nature, Stephanie Harry is not a politician, but the social worker has become an advocate for children with FAODs. "Some parents don't want to talk about their child's special needs," she says. "But I think the more I talk, the more helpful it will be."

She has written a book to help children and their parents better understand LCHAD deficiency and to cope with daily life. Emory's medical school supported its publication, and Harry is now receiving requests to have the book translated into Spanish and Hindi.

Brightly colored with a cartoon version of Christopher on the cover, My Special Body includes poems, activities, and illustrations to help children understand LCHAD deficiency and related FAODs. One page shows caterpillars of different lengths to help children learn how fats come in short, medium, long, and very long chain sizes. Using simple rhymes—"If I eat too much fat or not enough food, I get really tired and in a bad mood"—the book gives parents a way to start difficult conversations with their children about living with FAODs. Harry also hopes the book will ease the stigma for children with metabolic disorders.

"If you put it in a book, it normalizes the situation," says Harry. Then she looks at Christopher and adds, "It's like, he's your kid. You want the best for him. You don't want him to be defined by his condition."

The Harrys also are committed to raising research funds for LCHAD deficiency and other FAODs. This year, they competed in an Atlanta triathlon to raise $10,000 to support research at the Emory genetics metabolic nutrition clinic. "There hasn't been a lot of funding for rare inherited diseases," says Stephanie Harry, "but even with the small amount of research, these kids have done phenomenally well."

Christopher trained with his parents in a specially outfitted stroller they pushed while they prepared for the three-mile run, 400-yard swim, and 15-mile bike race. Then he watched from the sidelines as they competed.

At the end of the race, Stephanie Harry asked her son: "Do you understand why we ran the race?"

 "You have to help Dr. Singh," he answered. "She helps me."  EH

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