| Eligibility |
- INCLUSION CRITERIA:
All patients who meet clinical diagnostic criteria for PS, or who have demonstrated AKT1
p.Glu17Lys mutations are considered eligible for this protocol. As well, we will generally
offer an in-person evaluation at the NIHCC to patients with PS whenever possible.
As these disorders are usually apparent at or soon after birth, and appear to evolve at
least into the third decade of life, early assessment and long-term follow-up are
necessary. We have already learned that PS has a high pediatric mortality rate. PS and
other overgrowth disorders are progressive and for some individuals, may warrant more
frequent observation during youth and adolescence. Therefore, it would not be practicable
or ethical to exclude children from enrollment.
Patients with overgrowth that is not definitively PS (i.e., who do not appear to meet
clinical diagnostic criteria) may also be eligible to participate in this study. Decisions
to invite patients in this group to the NIHCC for an in-person evaluation are made on a
case-by-case basis where the patient s phenotype, health, proximity to the NIH, and fit
with our current research aims will all be taken into account. In general, we will consider
subjects who have one or more of the manifestations from the PS clinical criteria as
eligible.
Enrollment of adults with impaired decision-making capacity is scientifically justified
because PS is an ultra-rare disorder where 10-15% of patients have significant cognitive
impairment and gaining a better understanding of this aspect of the phenotype (as well as
the other concerns adult patients may present with) is critical to advancing our knowledge
of this disorder. Progression of overgrowth, particularly the fibroadipose overgrowth in
CLOVES syndrome, is a significant issue in many adults with this condition and
understanding the trajectory of overgrowth throughout the lifespan is an important goal of
this study.
This protocol enrolls participants of all ages which includes women of child-bearing age.
We recognize that women may become pregnant during the course of this study. While we have
not documented a case of a female with Proteus syndrome becoming pregnant it is important
to gather clinical data if such a case occurs in order to better understand the natural
history of Proteus syndrome and related disorders.
Since we enroll people of all ages, some of the women we enroll may become pregnant during
the course of the study. No radiation imaging studies will be done on women if they are
known to be pregnant. We will screen all women of reproductive age with a pregnancy test
prior to surgery, as per standard surgical practice.
There are no exclusions for race, age, or gender for participants.
EXCLUSION CRITERIA:
Patients with cancer but who do not have overgrowth or other non-tumor manifestations of PS
or non-PS overgrowth, whose tumors may harbor AKT1, PIK3CA, or other mutations, are not
eligible for this study. In general, patients who clearly meet diagnostic criteria for a
well-characterized overgrowth syndrome that is NOT PS are not eligible for this study.
Bannayan-Riley-Ruvalcaba syndrome and PHACES syndrome are examples of such entities. We
will not enroll prisoners, healthy volunteers, or lab personnel. Some persons with PS and
other overgrowth conditions are intellectually disabled (ID) or developmentally delayed
(probably ~10%). The consent issues are no different for children with ID than
developmentally appropriate children except that assent will be judged by developmental
level instead of age. Patients who are adults and decisionally-impaired are eligible only
if they have a legal guardian who has authority to sign a consent form on their behalf.
Patients who are medically fragile or unable to tolerate travel to the NIHCC will not
routinely be eligible for participation.
We will request permission to retain some information about prospective participants who
may not be immediately enrolled. As these participants will not immediately be signing a
consent form and joining the study, we propose to NOT count these participants in our
Inclusion Enrollment Reports until they have formally enrolled in the study (that is, they
have signed consent forms).
We will not enroll neonates (newborns less than one month old).
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