ESPE Abstracts (2019) 92 P3-198

A Rare Cause of Hypogonadotropic Hypogonadism: FGFR1Mutation

İbrahim Mert Erbas1, Ahu Paketçi1, Sezer Acar1, Damla Kotan2, Korcan Demir1, Ayhan Abaci1, Ece Böber1

1Dokuz Eylul University, Faculty of Medicine, Department of Pediatric Endocrinology, İzmir, Turkey. 2Çukurova University, Faculty of Medicine, Department of Pediatric Endocrinology, Adana, Turkey

Introduction: Mutations in FGFR1, which is involved in formation and migration of neurons responsible for the production of gonadotropin-releasing hormones, may either cause isolated hypogonadotropic hypogonadism (HH) or Kallmann syndrome (KS). In addition, FGFR1mutations were reported in 2.7% of the cases with multiple pituitary hormone deficiency.

Case: A 16-year-old male was referred to our clinic with absence of pubic hair and micropenis. He had a history of surgery for bilateral undescended testes. He was adopted in neonatal period, his birth and family history could not be reached. His weight was at -2.62 SDS, height -2.72 SDS, BMI -1.12 SDS. He had flat nasal root, Tanner Stage 3 pubic hair, testicular volumes were 2 ml on the left, 0.5 ml on the right, and stretched penile length was 2 cm. Laboratory results were as follows: fT4 1.14 ng/dL (0.5-1.51 ng/dL), TSH 1.57 mIU/mL (0.38-5.33 mIU/mL), FSH 0.71 mIU/mL (1.3-19.3 mIU/mL), LH 0.08 mIU/mL (N>0.3 mIU/mL), total testosterone 0.49 ng/mL (2.59-8.16 ng/mL). Bone age was consistent with 13 years of age. Peak LH response during LHRH test was 4.75 IU/L (N, > 5 IU/L). Brain MRI was normal, no pituitary pathology was evident. There was no response to pubertal induction for two times, and low dose testosterone replacement was initiated. Growth velocity was low during the follow-up and insulin tolerance test showed low growth hormone (peak 1,36 ng/mL, N>7) and normal cortisol response to hypoglycemia. Whole exome analysis revealed a previously reported, heterozygous p.R622X mutation in FGFR1.

Conclusion: More than 25 genes have been identified to be associated with congenital HH. FGFR1 mutations are among of the causes of congenital HH and KS, which are inherited autosomal dominantly and can be accompanied by cleft palate, tooth agenesis, and bimanual synkinesis.It should be kept in mind that multiple anterior pituitary hormone deficiencies may be associated with FGFR1 mutations as well.

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