Novel Mutation in PTHLH Related to Brachydactyly Type E2 Initially Confused with Unclassical Pseudopseudohypoparathyroidism.
10.3803/EnM.2018.33.2.252
- Author:
Jihong BAE
1
;
Hong Seok CHOI
;
So Young PARK
;
Do Eun LEE
;
Sihoon LEE
Author Information
1. Department of Internal Medicine and Laboratory of Genomics and Translational Medicine, Gachon University College of Medicine, Incheon, Korea. shleemd@gachon.ac.kr
- Publication Type:Original Article
- Keywords:
Brachydactyly;
Pseudopseudohypoparathyroidism;
Parathyroid hormone like hormone;
Parathyroid hormone-related protein
- MeSH:
Alleles;
Brachydactyly*;
Carrier Proteins;
Congenital Abnormalities;
DNA;
Exome;
Fathers;
Fingers;
Foot;
Genetic Background;
Grandparents;
Hand;
Humans;
Metacarpal Bones;
Metatarsal Bones;
Mothers;
Parathyroid Hormone;
Parathyroid Hormone-Related Protein;
Penetrance;
Pseudopseudohypoparathyroidism*;
Toes
- From:Endocrinology and Metabolism
2018;33(2):252-259
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND: Autosomal-dominant brachydactyly type E is a congenital abnormality characterized by small hands and feet, which is a consequence of shortened metacarpals and metatarsals. We recently encountered a young gentleman exhibiting shortening of 4th and 5th fingers and toes. Initially, we suspected him having pseudopseudohypoparathyroidism (PPHP) because of normal biochemical parameters, including electrolyte, Ca, P, and parathyroid hormone (PTH) levels; however, his mother and maternal grandmother had the same conditions in their hands and feet. Furthermore, his mother showed normal biochemical parameters. To the best of our knowledge, PPHP is inherited via a mutated paternal allele, owing to the paternal imprinting of GNAS (guanine nucleotide binding protein, alpha stimulating) in the renal proximal tubule. Therefore, we decided to further analyze the genetic background in this family. METHODS: Whole exome sequencing was performed using genomic DNA from the affected mother, son, and the unaffected father as a negative control. RESULTS: We selected the intersection between 45,490 variants from the mother and 45,646 variants from the son and excluded 27,512 overlapping variants identified from the father. By excluding homogenous and compound heterozygous variants and removing all previously reported variants, 147 variants were identified to be shared by the mother and son. Variants that had least proximities among species were excluded and finally 23 variants remained. CONCLUSION: Among them, we identified a defect in parathyroid hormone like hormone (PTHLH), encoding the PTH-related protein, to be disease-causative. Herein, we report a family affected with brachydactyly type E2 caused by a novel PTHLH mutation, which was confused with PPHP with unclassical genetic penetrance.
