Literature DB >> 2001103

A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features.

S A Sanjad1, N A Sakati, Y K Abu-Osba, R Kaddoura, R D Milner.   

Abstract

Twelve infants (six boys, six girls) with severe hypocalcaemic tetany or convulsions were seen over a three year period. Nine patients were symptomatic in the newborn period. Their hypocalcaemia was associated with hyperphosphataemia and very low concentrations of immunoreactive parathyroid hormone. None of the babies suffered from congenital cardiac disease. Cell mediated immunity, measured in five patients, was normal. There were no chromosomal abnormalities but all patients shared several dysmorphic features including deep set eyes, microcephaly, thin lips, beaked nose tip, external ear anomalies, micrognathia, and depressed nasal bridge. Mental retardation of varying degree was found in all patients. All had severe intrauterine and postnatal growth retardation. Four patients have died. The remaining eight patients are on treatments with vitamin D and calcium supplements with no change in their growth pattern. We believe that this association of congenital hypoparathyroidism with severe growth failure and dysmorphism represents a new syndrome.

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Year:  1991        PMID: 2001103      PMCID: PMC1792808          DOI: 10.1136/adc.66.2.193

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  12 in total

1.  Familial nephrosis, nerve deafness, and hypoparathyroidism.

Authors:  A Y Barakat; J B D'Albora; M M Martin; P A Jose
Journal:  J Pediatr       Date:  1977-07       Impact factor: 4.406

2.  Silver-Russell syndrome with unusual findings.

Authors:  K K Hansen; L A Latson; B A Buehler; L A Latson
Journal:  Pediatrics       Date:  1987-01       Impact factor: 7.124

3.  Partial monosomy 10p syndrome.

Authors:  R Koenig; E Kessel; W Schoenberger
Journal:  Ann Genet       Date:  1985

4.  Familial isolated hypoparathyroidism: a molecular genetic analysis of 8 families with 23 affected persons.

Authors:  T G Ahn; S E Antonarakis; H M Kronenberg; T Igarashi; M A Levine
Journal:  Medicine (Baltimore)       Date:  1986-03       Impact factor: 1.889

5.  Short stature, mental retardation, and hypoparathyroidism: a new syndrome.

Authors:  R J Richardson; J M Kirk
Journal:  Arch Dis Child       Date:  1990-10       Impact factor: 3.791

6.  Kenny syndrome: evidence for idiopathic hypoparathyroidism in two patients and for abnormal parathyroid hormone in one.

Authors:  S Fanconi; J A Fischer; P Wieland; M Atares; A Fanconi; A Giedion; A Prader
Journal:  J Pediatr       Date:  1986-09       Impact factor: 4.406

7.  The association of the DiGeorge anomalad with partial monosomy of chromosome 22.

Authors:  R I Kelley; E H Zackai; B S Emanuel; M Kistenmacher; F Greenberg; H H Punnett
Journal:  J Pediatr       Date:  1982-08       Impact factor: 4.406

8.  The spectrum of the DiGeorge syndrome.

Authors:  M E Conley; J B Beckwith; J F Mancer; L Tenckhoff
Journal:  J Pediatr       Date:  1979-06       Impact factor: 4.406

9.  Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy.

Authors:  P J Dahlberg; W Z Borer; K L Newcomer; W R Yutuc
Journal:  Am J Med Genet       Date:  1983-09

10.  Partial monosomy of chromosome 10 short arms.

Authors:  A Gencík; U Brönniman; R Tobler; P Auf der Maur
Journal:  J Med Genet       Date:  1983-04       Impact factor: 6.318

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  36 in total

1.  Defective growth hormone secretion and hypogonadism in the new syndrome of congenital hypoparathyroidism, growth failure and dysmorphic features.

Authors:  A T Soliman; A Darwish; I alSalmi; M Asfour
Journal:  Indian J Pediatr       Date:  1996 Sep-Oct       Impact factor: 1.967

Review 2.  Genetics of endocrine and metabolic disorders: parathyroid.

Authors:  R V Thakker
Journal:  Rev Endocr Metab Disord       Date:  2004-03       Impact factor: 6.514

3.  Case report: Management of severe posterior open bite due to primary failure of eruption.

Authors:  J Mc Cafferty; E Al Awadi; A C O'Connell
Journal:  Eur Arch Paediatr Dent       Date:  2010-06

Review 4.  Endocrinological Manifestations of Sanjad-Sakati Syndrome.

Authors:  Masharib Bashar; Muhammad Taimur; Fnu Amreek; Khalid A Sayeed; Amber Tahir
Journal:  Cureus       Date:  2020-06-22

Review 5.  Genetic Disorders of Parathyroid Development and Function.

Authors:  Rebecca J Gordon; Michael A Levine
Journal:  Endocrinol Metab Clin North Am       Date:  2018-10-12       Impact factor: 4.741

6.  A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features.

Authors:  R J Richardson; J Kirk
Journal:  Arch Dis Child       Date:  1991-11       Impact factor: 3.791

7.  Hypoparathyroidism in the adult: epidemiology, diagnosis, pathophysiology, target-organ involvement, treatment, and challenges for future research.

Authors:  John P Bilezikian; Aliya Khan; John T Potts; Maria Luisa Brandi; Bart L Clarke; Dolores Shoback; Harald Jüppner; Pierre D'Amour; John Fox; Lars Rejnmark; Leif Mosekilde; Mishaela R Rubin; David Dempster; Rachel Gafni; Michael T Collins; Jim Sliney; James Sanders
Journal:  J Bone Miner Res       Date:  2011-10       Impact factor: 6.741

8.  Sanjad-Sakati Syndrome in Sudanese children.

Authors:  Wiam A Arabi; Areej A Basheer; Mohamed A Abdullah
Journal:  Sudan J Paediatr       Date:  2011

9.  Biallelic TBCD Mutations Cause Early-Onset Neurodegenerative Encephalopathy.

Authors:  Noriko Miyake; Ryoko Fukai; Chihiro Ohba; Takahiro Chihara; Masayuki Miura; Hiroshi Shimizu; Akiyoshi Kakita; Eri Imagawa; Masaaki Shiina; Kazuhiro Ogata; Jiu Okuno-Yuguchi; Noboru Fueki; Yoshifumi Ogiso; Hiroshi Suzumura; Yoshiyuki Watabe; George Imataka; Huey Yin Leong; Aviva Fattal-Valevski; Uri Kramer; Satoko Miyatake; Mitsuhiro Kato; Nobuhiko Okamoto; Yoshinori Sato; Satomi Mitsuhashi; Ichizo Nishino; Naofumi Kaneko; Akira Nishiyama; Tomohiko Tamura; Takeshi Mizuguchi; Mitsuko Nakashima; Fumiaki Tanaka; Hirotomo Saitsu; Naomichi Matsumoto
Journal:  Am J Hum Genet       Date:  2016-09-22       Impact factor: 11.025

10.  New Ocular Associations in Sanjad-Sakati Syndrome: Case report from Oman.

Authors:  Agha S Haider; Anuradha Ganesh; Adila Al-Kindi; Ahmad Al-Hinai; Nadia Al-Kharousi; Saif Al-Yaroubi; Sana Al-Zuhaibi
Journal:  Sultan Qaboos Univ Med J       Date:  2014-07-24
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