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. 2018 Jul 21:2018:18-0068.
doi: 10.1530/EDM-18-0068. eCollection 2018.

Brachydactyly mental retardation syndrome with growth hormone deficiency

Affiliations

Brachydactyly mental retardation syndrome with growth hormone deficiency

Alireza Arefzadeh et al. Endocrinol Diabetes Metab Case Rep. .

Abstract

Deletion of chromosome 2q37 results in a rare congenital syndrome known as brachydactyly mental retardation (BDMR) syndrome; a syndrome which has phenotypes similar to Albright hereditary osteodystrophy (AHO) syndrome. In this report, we describe a patient with AHO due to microdeletion in long arm of chromosome 2 [del(2)(q37.3)] who had growth hormone (GH) deficiency, which is a unique feature among reported BDMR cases. This case was presented with shortening of the fourth and fifth metacarpals which along with AHO phenotype, brings pseudopseudohypoparathyroidism (PPHP) and pseudohypoparathyroidism type Ia (PHP-Ia) to mind; however, a genetic study revealed del(2)(q37.3). We recommend clinicians to take BDMR in consideration when they are faced with the features of AHO; although this syndrome is a rare disease, it should be ruled out while diagnosing PPHP or PHP-Ia. Moreover, we recommend evaluation of IGF 1 level and GH stimulation test in patients with BDMR whose height is below the 3rd percentile.

Learning points: Clinicians must have brachydactyly mental retardation (BDMR) syndrome in consideration when they are faced with the features of Albright hereditary osteodystrophy.Although BDMR syndrome is a rare disease, it should be ruled out while diagnosing PPHP or PHP-Ia.Evaluation of IGF1 level in patients diagnosed with BDMR whose height is below the 3rd percentile is important.

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Figures

Figure 1
Figure 1
Apparent shortening of 4th and 5th metacarpals and metatarsals in patient’s hands (A) and feet (B), respectively.
Figure 2
Figure 2
Plain radiograph studies of left foot and hand.
Figure 3
Figure 3
Growth and weight chart.

References

    1. Online Mendelian Inheritance in Man O. MIM Number: 600430. Baltimore, MD: Johns Hopkins University.
    1. Williams SR, Aldred MA, Der Kaloustian VM, Halal F, Gowans G, McLeod DR, Zondag S, Toriello HV, Magenis RE, Elsea SH. Haploinsufficiency of HDAC4 causes brachydactyly mental retardation syndrome, with brachydactyly type E, developmental delays, and behavioral problems. American Journal of Human Genetics 2010. 87 219–228. (https://doi.org/10.1016/j.ajhg.2010.07.011) - PMC - PubMed
    1. Hacıhamdioğlu B, Arslan M, Sarı E, Kurtçu K, Yesilkaya E. Brachydactyly mental retardation syndrome in differential diagnosis of pseudopseudohypoparathyroidism. Journal of Pediatric Endocrinology and Metabolism 2013. 26 793–795. (https://doi.org/10.1515/jpem-2012-0375) - PubMed
    1. Goswami M, Verma M, Singh A, Grewal H, Kumar G. Albright hereditary osteodystrophy: a rare case report. Journal of Indian Society of Pedodontics and Preventive Dentistry 2009. 27 184 (https://doi.org/10.4103/0970-4388.57101) - PubMed
    1. Reeder MM, Bradley WGJ, Merritt CR. Reeder and Felson’s Gamuts in Radiology: Comprehensive Lists of Roentgen Differential Diagnosis. New York: Springer, 2003.