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A case of Aromatase deficiency due to a novel CYP19A1 mutation.
[aromatase deficiency]
Aromatase
deficiency
is
a
rare
,
autosomal
recessive
disorder
of
which
there
are
approximately
twenty
four
case
reports
.
The
aromatase
enzyme
is
crucial
in
the
biosynthesis
of
oestrogens
from
androgens
.
The
phenotype
of
aromatase
deficiency
therefore
is
the
result
of
androgen
excess
and
oestrogen
deficiency
in
the
absence
of
normal
aromatase
activity
.
We
report
the
first
case
of
aromatase
deficiency
diagnosed
in
a
female
adult
,
at
the
age
of
32
Â
years
,
due
to
a
novel
duplication
in
the
aromatase
gene
.
A
32
Â
year
old
Indian
woman
presented
with
a
history
of
gender
assignment
difficulties
at
birth
,
lack
of
pubertal
development
,
osteopaenia
with
fracture
and
tall
stature
.
She
had
central
obesity
,
impaired
fasting
glucose
and
borderline
hypertension
.
Past
examinations
had
revealed
partial
fusion
of
urethra
and
vagina
,
hypoplastic
uterus
and
streak
ovaries
.
The
ovaries
had
been
excised
due
to
malignant
risk
after
an
initial
clinical
diagnosis
of
Turner
's
syndrome
with
Y
mosaicism
.
Oestrogen
replacement
commenced
shortly
after
her
fracture
,
in
adulthood
.
After
reassessment
,
aromatase
deficiency
was
diagnosed
.
Sequencing
of
the
coding
exons
of
the
aromatase
(
CYP
19
A
1
;
OMIM
109710
)
gene
revealed
a
novel
27
-
base
duplication
in
exon
8
(
p
.
Ala
306
_
Ser
314
dup
)
.
This
duplication
,
occurring
within
the
aromatase
α-
helix
,
would
be
likely
to
disrupt
substrate
(
androgen
)
and
cofactor
(
protoporphyrin
IX
)
binding
,
resulting
in
a
lack
of
oestrogen
synthesis
.
We
report
a
female
with
a
phenotype
compatible
with
aromatase
deficiency
which
was
unrecognised
until
adulthood
and
found
she
had
a
novel
duplication
in
CYP
19
A
1
.
Previous
case
reports
have
described
polycystic
ovarian
morphology
,
especially
in
childhood
and
adolescence
,
but
never
streak
ovaries
.
This
may
reflect
the
few
adult
cases
reported
,
that
aromatase
deficiency
in
females
is
generally
diagnosed
at
birth
and
oestrogen
treatment
commences
decades
earlier
than
occurred
in
our
patient
.
Streak
ovaries
are
consistent
with
the
phenotype
of
the
aromatase
knockout
mouse
followed
through
adulthood
.
The
observed
clinical
features
of
obesity
,
dysglycaemia
and
hypertension
,
are
compatible
with
the
observation
that
lack
of
a
counterbalancing
effect
of
oestrogen
on
tissue
androgens
until
adulthood
may
lead
to
a
metabolic
syndrome
phenotype
.
This
report
broadens
the
spectra
of
phenotype
and
genetic
mutations
underlying
this
rare
disorder
.
Diseases
Validation
Diseases presenting
"tall stature"
symptom
achondroplasia
aromatase deficiency
cohen syndrome
This symptom has already been validated