ESPE Abstracts

ESPE Abstracts

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61st Annual ESPE (ESPE 2023)

The Hague, Netherlands
21 Sept 2023 - 23 Sept 2023

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The 61st ESPE Annual Meeting will now be taking place in The Hague, The Netherlands

Poster Category 2

Adrenals and HPA Axis

Table of contents
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Bone, Growth Plate and Mineral Metabolism

hrp0097p2-3 | Adrenals and HPA Axis

Glucocorticoid induced adrenal insufficiency evaluated by the low dose short corticotropin test in children

hrp0097p2-4 | Adrenals and HPA Axis

Newborn screening for 21 OH Congenital adrenal hyperplasia in Italy: a 14 years population study.

hrp0097p2-42 | Adrenals and HPA Axis

Exploring the Experiences of Parents of Children with Congenital Adrenal Hyperplasia: a study in Developing Country

hrp0097p2-76 | Adrenals and HPA Axis

The genotype-phenotype correlations in patients with 21-hydroxylase deficiency in Henan, China and the relationship between the clinically effective dosage of hydrocortisone and CYP21A2 genotype

hrp0097p2-77 | Adrenals and HPA Axis

Massive adrenocortical carcinoma with right atrium invasion in a two-year old girl with li fraumeni syndrome – possibility of succesful ressection after neoadjuvant chemotherapy

hrp0097p2-78 | Adrenals and HPA Axis

Massive adrenocortical carcinoma with right atrium invasion in a two-year old girl with Li Fraumeni syndrome – possibility of succesful ressection after neoadjuvant chemotherapy

hrp0097p2-79 | Adrenals and HPA Axis

Final Adult Height in Saudi patients with Congenital Adrenal Hyperplasia

hrp0097p2-80 | Adrenals and HPA Axis

Cortisol and 11-oxygenated androgens in hair samples from children and adolescents with congenital adrenal hyperplasia

hrp0097p2-139 | Adrenals and HPA Axis

A 6-year-old boy with Duchenne Muscular Dystrophy and acute adrenal insufficiency: a case report

hrp0097p2-140 | Adrenals and HPA Axis

Testicular Adrenal Rest Tumors (TARTs) as presenting symptom of CAH due to CYP11A1deficiency.

hrp0097p2-141 | Adrenals and HPA Axis

Pediatric Cushing Disease: a single center experience

hrp0097p2-155 | Adrenals and HPA Axis

A case of Ectopic ACTH in a girl with thymic carcinoid

hrp0097p2-156 | Adrenals and HPA Axis

Aldosterone deficiency and resistance: The different faces of renal salt loss

hrp0097p2-157 | Adrenals and HPA Axis

ACTH-independent hypercortisolemia: onset clinical picture in a 10-year-old boy with Carney complex

hrp0097p2-160 | Adrenals and HPA Axis

Factors Influencing the Final Height of Congenital Adrenal Hyperplasia Patients

hrp0097p2-168 | Adrenals and HPA Axis

Cushing’s Disease: an Example of Drug Shortage’s Impact in Pediatric Endocrinology.

hrp0097p2-169 | Adrenals and HPA Axis

Von Hippel-Lindau syndrome in a 9-year-old boy

hrp0097p2-186 | Adrenals and HPA Axis

Severe hypertension with hypokalemia in uncompliance child with CAH: Fludrocortisone a cause of HTN.

hrp0097p2-187 | Adrenals and HPA Axis

Challenges and barriers of choosing the sex in patients with congenital adrenal hyperplasia: a case report

hrp0097p2-188 | Adrenals and HPA Axis

7-year-old girl as compound heterozygote of non-classic congenital adrenal hyperplasia

hrp0097p2-189 | Adrenals and HPA Axis

A rare case of a newborn with congenital adrenal hyperplasia, osteogenesis imperfect and cow’s milk allergy

hrp0097p2-190 | Adrenals and HPA Axis

Evaluation of two cases with 46,XX and 46,XY karyotypes diagnosed with 17α-hydroxylase deficiency

hrp0097p2-191 | Adrenals and HPA Axis

Should we routinely assess hypothalamo-pituitary-adrenal axis in pediatric patients with Prader-Willi Syndrome?

hrp0097p2-192 | Adrenals and HPA Axis

Neonatal CAH screening in patients with rare causes of inherited primary adrenal insufficiency

hrp0097p2-193 | Adrenals and HPA Axis

Patient with Carney complex syndrome due to PRKAR1A mutation.

hrp0097p2-202 | Adrenals and HPA Axis

Rare Association of 11 Beta Hydroxylase Deficiency and Gitelman Syndrome and Overlapping Symptoms

hrp0097p2-203 | Adrenals and HPA Axis

A male infant with X- linked congenital adrenal hypoplasia and Xp 21 contiguous gene deletion syndrome- case report

hrp0097p2-212 | Adrenals and HPA Axis

A rare case of Aldosterone synthase deficiency presenting with Hypertension.

hrp0097p2-213 | Adrenals and HPA Axis

Pseudohypoaldosteronism in congenital anomaly of the kidneys and urinary tract – case presentation

hrp0097p2-214 | Adrenals and HPA Axis

APECED and COVID 19: Two Case Reports

hrp0097p2-215 | Adrenals and HPA Axis

Pseudocushing. an exceptional patology in pediatrics

hrp0097p2-216 | Adrenals and HPA Axis

Non classic congenital adrenal hyperplasia caused by mutations in CYP21A2

hrp0097p2-217 | Adrenals and HPA Axis

Primary hypoaldosteronism due to aldosterone synthase deficiency in a small for gestational age born infant

hrp0097p2-218 | Adrenals and HPA Axis

Early manifestation of primary adrenal insufficiency in patients with X-linked adrenoleukodystrophy: clinical cases description

hrp0097p2-219 | Adrenals and HPA Axis

Osteoporosis as the first sign of Cushing disease - a case report

hrp0097p2-220 | Adrenals and HPA Axis

A Case of Adrenal Suppression Secondary to Intranasal Betamethasone

hrp0097p2-221 | Adrenals and HPA Axis

Diabetes insipidus as first manifestation of congenital malformation of the neurocranium

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