{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,18]],"date-time":"2025-10-18T10:19:31Z","timestamp":1760782771665},"reference-count":21,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2005,6,7]],"date-time":"2005-06-07T00:00:00Z","timestamp":1118102400000},"content-version":"vor","delay-in-days":3932,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1994,9]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>A 5 1\/2\u2010year\u2010old Saudi Arabian girl presented with a syndrome of intrauterine growth retardation, minor anomalies, hypoparathyroidism, and growth hormone deficiency. She was the product of a consanguineous mating. Her minor anomalies and delayed development were similar to findings in a previously reported Saudi Arabian patients with hypoparathyroidism and growth deficiency. There were substantial differences in findings from a series of Kuwaiti children. Parathyroid hormone was undetectable, but the renal response to infused parathyroid hormone was normal, indicating primary hypoparathyroidism. In response to arginine stimulation, her GH rose to 5.8 ng\/ml (5.8 \u03bcg\/L) (nl &gt; 10), and to 2.3 ng\/ml (2.3 \u03bcg\/L) after L\u2010dopa. Following clonidine it rose to 15 ng\/ml (15 \u03bcg\/L) at 120 minutes. She responded normally to infusions of GHRH (GH rose to 22 ng\/ml (22 \u03bcg\/L) at 75 minutes) and TRH (TSH rose to 37 \u03bcu\/ml, 37 mlU\/L). On treatment with recombinant human growth hormone, she showed an increase in height and weight. Hypocalcemia was well controlled with supplemental 1\u2010\u03b1\u2010cholecalciferol. \u00a9 1994 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.1320520316","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T17:17:14Z","timestamp":1118510234000},"page":"334-338","source":"Crossref","is-referenced-by-count":19,"title":["Syndrome of hypoparathyroidism, growth hormone deficiency, and multiple minor anomalies"],"prefix":"10.1002","volume":"52","author":[{"given":"Deborah","family":"Marsden","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"William L.","family":"Nyhan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nadia O.","family":"Sakati","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2005,6,7]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1097\/00005792-198603000-00001"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1172\/JCI114811"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.2214\/ajr.100.1.1"},{"key":"e_1_2_1_5_1","doi-asserted-by":"publisher","DOI":"10.1210\/jcem-62-3-466"},{"key":"e_1_2_1_6_1","doi-asserted-by":"publisher","DOI":"10.1210\/jcem-57-6-1145"},{"key":"e_1_2_1_7_1","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1542\/peds.79.1.125","article-title":"Silver\u2010Russell syndrome with unusual findings","volume":"79","author":"Hansen KK","year":"1987","journal-title":"Pediatrics"},{"key":"e_1_2_1_8_1","first-page":"88","volume-title":"Smith's Recognizable Patterns of Human Malformation","author":"Jones KL","year":"1988"},{"key":"e_1_2_1_9_1","doi-asserted-by":"publisher","DOI":"10.1001\/archpedi.1966.02090050133013"},{"key":"e_1_2_1_10_1","doi-asserted-by":"publisher","DOI":"10.1203\/00006450-199110000-00006"},{"key":"e_1_2_1_11_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320140419"},{"key":"e_1_2_1_12_1","first-page":"6372","article-title":"Gene encoding human growth hormone\u2010releasing factor precursor: Structure, sequence and chromosomal assignment","volume":"78","author":"Mayo KE","year":"1981","journal-title":"Proc Natl Acad Sci U S A"},{"key":"e_1_2_1_13_1","volume-title":"Mendelian Inheritance. 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