Professional Documents
Culture Documents
44 GH
44 GH
44 GH
A 11-year-old girl presents to your clinic for evaluation of short stature. Parents report
that she has always been the shortest girl in her class, but they have become concerned
because the patient's 8-year-old sister is now the same height as she is. The patient has
not yet attained menarche and her mother reports no breast development. She has been
well with no chronic medical problems, no hospitalizations, and no surgeries. She lives
with her mother, father, and sister and she is currently a student in the fifth grade with
excellent school performance. Her mother is 173 cm. She had menarche at age 12. The
patient's father is 185 cm. He started shaving at age 15. There is no family history of any
medical problems.
Tanner 1 breasts.
Her growth chart is reviewed which demonstrates her growth velocity of 3 cm per year.
Bone age 9 years and 6 months. CBC, ESR, TFT's, celiac screen, Urea and serum
electrolytes are normal.
Q2: What is your possible diagnosis and how do you confirm it?
The patient's father is 175 cm. He started shaving at age 17 and he has history pf SS when
he was at preparatory school.
Q2: Which laboratory tests do you think are needed to refine the diagnosis?
An eight-year-old girl presents to your clinic for evaluation of short stature. Her parents
reported 3years of growth arrest, during which she continued to wear the same size of
clothing and fell well below the third percentile for height. Previous growth velocity had
been normal. she born at term after an uneventful pregnancy with a birth weight of 3700
g. she has been well with no chronic medical problems, no hospitalizations, and no
surgeries. she lives with her mother, father, and sister and he is currently a student in the
third grade with very good school performance
Breast development began at seven- and 6-months years of age with scant pubic hair that
developed shortly thereafter.
Her mother is 170 cm. She had menarche at age 12. The patient's father is 175 cm. He
started shaving at age 15. There is no family history of any medical problems.
Investigations revealed CBC, ESR, celiac screen, Urea and serum electrolytes are normal.
TSH level of 1.3 mIU/L (normal range 0.5 mIU/L to 5 mIU/L) and fT4) 8.2 pmol/L
(normal range 8.7 pmol/L to 16 pmol/L).
Growth hormone (GH) stimulation testing with insulin and clonidine revealed peak GH
levels of only 2.4 μg/L and 1.7 μg/L, respectively (normal ≥5.6 μg/L).
LH and FSH levels were only 1 IU/L and 5 IU/L, respectively, a gonadotropin-releasing
hormone stimulation test demonstrated a peak luteinizing hormone level of 11 IU/L,
confirming gonadotropin-dependent (central) puberty.
She was diagnosed with GH deficiency (GHD), central precocious puberty and
central hypothyroidism.