research toward identifying the HRD gene took place in the molecular
and developmental genetics laboratory of BGU's Faculty of Health
sciences and the Soroka University Medical Center
Israeli researchers are playing
an important role in identifying a defective gene that causes a rare and
usually fatal disease in Arab infants.
The study is the result of a unique arrangement in which an American scientist
is coordinated the work of the Israelis at Ben-Gurion University of the
Negev, together with parallel research by Saudi Arabian and Kuwaiti scientists.
This means that the Arabs were not actually "collaborating" directly with
their Israeli colleagues, yet still allowed their findings to be pooled,
which paved the way for the comprehensive understanding of the disease
that led to the identification of the gene.
The findings of the study on the gene were published jointly in Nature
Genetics a few
months ago, using research that was carried out without any contact between
the Arabs and the Israelis. Dr. George Diaz of Mount Sinai Hospital in
New York City served as the coordinator, transmitting data to the various
sets of researchers in order to eliminate the need for them to communicate
The findings benefit Arabs alone: this gene affects, among others, the
Palestinian and Bedouin populations in Israel, who were studied in the
"Our first priority is to help and treat the Bedouins of the Negev," Dr.
Ruti Parvari told Israel 21c. Parvari is a member of the molecular and
developmental genetics department of BGU's Health Sciences Faculty and
on staff Soroka Hospital in Beersheba. "At the same time, they are a unique
population with certain genetic diseases not found in the general population.
Information they can provide helps us identify genes and learn more about
the biological processes they trigger."
The recessive gene causing hypoparathyroidism retardation and dysmorphism
(HRD) was found on chromosome No. 1 in 35 Arab families in the Negev,
Saudi Arabia, and Kuwait. In addition, a French physician reported on
a case in a Moroccan family and another was found in a patient in Belgium.
The findings indicate that a single Arab was the source of the gene mutation
decades or perhaps centuries ago.
The discovery opens an opportunity for a deeper understanding of the cellular
biology involved in the disease and makes prenatal diagnosis possible,
Parvari told the Jerusalem Post, which reported on this story after the
Nature Genetics article appeared.
The disease caused by the gene involves severe calcium deficiency that
results in abnormally low birth weight, mental retardation, very slow
physical growth, and a tendency to seizures. The disease has been compared
to Tay-Sachs, a genetic disease found among Ashkenazi Jews.
A number of Israeli Bedouin families have taken advantage of prenatal
diagnosis and have already aborted fetuses carrying the gene.
"We know that the Bedouins have a great religious difficulty with abortion,"
said Parvari. "Our hope is that we can eventually find a way to prevent
or treat the condition."
All of the Arab couples studied by the BGU team were first or second cousins
who married. Thus, increasing education to discourage inter-family unions
is a possible directions towards preventing the genetic condition.
The research began when Soroka pediatricians Dr. Eli Hershkovitz and Prof.
Rafael Gorodicher diagnosed children with HRD and found that it was a
rare disorder passed on by parents who were non-symptomatic carriers of
the gene. Every pregnancy of such couples has a 25 percent risk of an
HRD baby. Parvari performed the molecular research on blood tests taken
from the patients and their families.
At the same time, a team headed by Diaz in Manhattan published research
describing a similar syndrome with the same chromosomal location as that
found in affected Arab families in Saudi Arabia and Kuwait. Diaz, a human
geneticist focusing on skeletal diseases, was eager to mediate the research.
Knowing that scientists from the Arab countries were not permitted to
be in contact with Israelis, even by e-mail, Diaz volunteered as coordinator
of the project that found the exact location of the gene.
Putting all of the findings together was crucial, since the larger number
of individuals who took part in the genetic study increased the accuracy
of finding the exact section of the chromosome where the gene is located.