Brooke Greenberg | |
|---|---|
 | |
| Born | Brooke Megan Greenberg (1993-01-08)January 8, 1993 |
| Died | October 24, 2013(2013-10-24) (aged 20) Baltimore, Maryland, United States |
| Cause of death | Bronchomalacia |
| Known for | Syndrome X |
Brooke Megan Greenberg (January 8, 1993 – October 24, 2013)[1][2] was an American woman who became famous for being the first documented case ofneotenic complex syndrome. Throughout her life of 20 years, she remained physically and cognitively similar to atoddler despite her increasing age. She was about 30 in (76 cm) tall, weighed about 16 lb (7.3 kg), and had an estimatedmental age of nine months to one year.
Brooke was born on January 8, 1993,[1][3] to parents Howard and Melanie Greenberg[4] atSinai Hospital inBaltimore, Maryland. She was delivered bycaesarean section, one month before her due date due to "intermittent growth",[5] weighing just four pounds (1.8 kg). She was born withanterior hip dislocation, a condition that caused her legs to be swiveled upward toward her shoulders; it was corrected surgically. Otherwise, Brooke appeared to be a typical infant.[6] She was the third of four girls born to her parents.[5]
In her first six years, she went through a series of unexplainedmedical emergencies from which she recovered. She had seven perforatedstomach ulcers. She also had aseizure. This was followed by what was later diagnosed as astroke; weeks later, no damage was detected. At age five, Brooke had a mass in her brain that caused her to go into a deep sleep (after confirmation that it was not acoma) for 14 days. The doctors diagnosed the mass as abrain tumor. She later awoke, and physicians found no tumor present. Brooke's pediatrician, Dr. Lawrence Pakula, stated that the source of her sudden illness remains a mystery.[7]
During an interview on the talk showKatie, her father stated that, between the ages of four and five, she stopped growing.[8]Child Frozen In Time, a documentary about Brooke,[5] was first broadcast onTLC on August 9, 2009.[9]
Over several years, the Greenbergs visited many specialists, looking for an explanation for their daughter's strange condition, yet there was no diagnosis of any known genetic syndrome or chromosomal abnormality.[10] In 2001, whenDateline documented Brooke at eight years of age, she was still the size of a six-month-old infant, weighing just 13 lb (5.9 kg) at 30 inches (76 cm) tall. The family still had no explanation. Brooke's mother Melanie said, "They [the specialists] just said she'll catch up. Then we went to thenutritionist, theendocrinologist. We tried thegrowth hormone…". The growth hormone treatment had no effect. Howard, Brooke's father, said, "I mean, she did not put on an ounce, or she did not grow an inch... That's when I knew there was a problem." After the growth hormone administration failed, the doctors, unable todiagnose a known condition, named her conditionSyndrome X.
The Greenbergs made many visits to nearbyJohns Hopkins Children's Center and even took Brooke to New York'sMount Sinai Hospital, searching for information about their daughter's condition.[6] Whengeneticists sequenced Greenberg'sDNA, they found that thegenes associated with thepremature aging diseases were normal, unlike themutated versions in patients withWerner syndrome andprogeria.[11]
In 2006, Richard Walker, an endocrine physiologist at theUniversity of South Florida College of Medicine, said that Brooke's body was not developing as a coordinated unit but as independent parts that were out of synchronization.[12][failed verification][13][14] She was never diagnosed with any knowngenetic disorder orchromosomal abnormality that would help explain why.[7] Hertelomeres seemed to be shortening at the normal rate.[10]
In 2009, Walker said, "There've been very minimal changes in Brooke's brain … Various parts of her body, rather than all being at the same stage, seem to be disconnected."[7] Walker noted that Brooke's brain, for example, was not much more mature than that of a newborn infant. He estimated her mental age at around nine months to a year old. Brooke could make gestures and recognize sounds but could not speak. Her bones were like those of a ten-year-old, and she still had herbaby teeth, which had an estimated developmental age of about eight years. Said Walker, "We think that Brooke's condition presents us with a unique opportunity to understand the process of aging."[15] "Different parts of her body are developing at different rates, as if they were not a unit but parts of separate organisms," Walker explained.[1]
Brooke Greenberg died on October 24, 2013, at the Herman and Walter Samuelson Children's Hospital at Sinai Medical Center in Baltimore, the same hospital where she was born. Her funeral service took place on October 27, 2013, and that same morning, she was buried at Baltimore Hebrew Cemetery - Berrymans Lane, inReisterstown,Maryland.[2] The cause of her death wasbronchomalacia, a medical condition usually occurring in children, which results in difficulty breathing due to weak cartilage in the walls of thebronchial tubes.[16]
In May 2015, it was reported that Layla Qualls of Oklahoma looked as if she was 9 or 10 months old, but was 3 years old. She was among seven children worldwide with Syndrome X that are being studied by researchers at theUniversity of California, Los Angeles. She died on January 7, 2020, at the age of 7.In their ongoing research they found that the blood of Syndrome X children appears to age normally.[17] Layla was also featured in a TLC documentary titled "The Girls Who Don't Age". This documentary aired July 18, 2016 on TLC.[18]
In July 2016, it was reported that Alyssa Pennington of New Mexico looks as if she is five years old, but is 12 years old.[18] She is another Syndrome X case.[19]
Another case that has been reported in July 2016 is Jenifer Sandoval of Colorado. Although she looks as if she is four years old, she is 22 years old.[18][20]
Blood tissue from five other female Syndrome X cases (whose average age was 6.3 years) turned out to be age-appropriate[21] according to a biomarker of aging known asepigenetic clock. The mean epigenetic age of the five pure Syndrome X subjects was 6.7 years (standard error=1.0) which is not significantly different from the mean chronological age of 6.3 years (standard error=1.8). Notably, the oldest pure Syndrome X case had an epigenetic age of 14.5 years which was 3.2 years older than her true chronological age. It is not yet known whether the epigenetic age of other tissues is also age appropriate in these cases.
Blood samples from each of the "Syndrome X" girls were sent to Dr. Radoje Drmanac in San Francisco, who did a full genomic sequencing and found the common link shared by the girls, leading the syndrome to be renamed "neotenic complex syndrome".[22][23]
