U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Postnatal onset growth deficiency

MedGen UID:
347476
•Concept ID:
C1857534
•
Finding

Professional guidelines

PubMed

Challenges in the Management of Short Stature.
Argente J
Horm Res Paediatr 2016;85(1):2-10. Epub 2015 Dec 10 doi: 10.1159/000442350. PMID: 26649429
Neonatal management and long-term sequelae.
Halliday HL
Best Pract Res Clin Obstet Gynaecol 2009 Dec;23(6):871-80. Epub 2009 Jul 26 doi: 10.1016/j.bpobgyn.2009.06.005. PMID: 19632899
Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency.
Hoffmann GF, Athanassopoulos S, Burlina AB, Duran M, de Klerk JB, Lehnert W, Leonard JV, Monavari AA, Müller E, Muntau AC, Naughten ER, Plecko-Starting B, Superti-Furga A, Zschocke J, Christensen E
Neuropediatrics 1996 Jun;27(3):115-23. doi: 10.1055/s-2007-973761. PMID: 8837070

Recent clinical studies

Etiology

A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter-->22q12.1: clinical, cytogenetic and molecular observations.
Vaglio A, Milunsky A, Huang XL, Quadrelli A, Mechoso B, Maher TA, Quadrelli R
Eur J Med Genet 2008 Jul-Aug;51(4):332-42. Epub 2008 Jan 25 doi: 10.1016/j.ejmg.2008.01.001. PMID: 18316257

Diagnosis

Mild Brachmann-de Lange syndrome. Delineation of the clinical phenotype, and characteristic behaviors in a six-year-old boy.
Bay C, Mauk J, Radcliffe J, Kaplan P
Am J Med Genet 1993 Nov 15;47(7):965-8. doi: 10.1002/ajmg.1320470706. PMID: 7507294

Prognosis

A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter-->22q12.1: clinical, cytogenetic and molecular observations.
Vaglio A, Milunsky A, Huang XL, Quadrelli A, Mechoso B, Maher TA, Quadrelli R
Eur J Med Genet 2008 Jul-Aug;51(4):332-42. Epub 2008 Jan 25 doi: 10.1016/j.ejmg.2008.01.001. PMID: 18316257
Mild Brachmann-de Lange syndrome. Delineation of the clinical phenotype, and characteristic behaviors in a six-year-old boy.
Bay C, Mauk J, Radcliffe J, Kaplan P
Am J Med Genet 1993 Nov 15;47(7):965-8. doi: 10.1002/ajmg.1320470706. PMID: 7507294

Clinical prediction guides

A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter-->22q12.1: clinical, cytogenetic and molecular observations.
Vaglio A, Milunsky A, Huang XL, Quadrelli A, Mechoso B, Maher TA, Quadrelli R
Eur J Med Genet 2008 Jul-Aug;51(4):332-42. Epub 2008 Jan 25 doi: 10.1016/j.ejmg.2008.01.001. PMID: 18316257
Mild Brachmann-de Lange syndrome. Delineation of the clinical phenotype, and characteristic behaviors in a six-year-old boy.
Bay C, Mauk J, Radcliffe J, Kaplan P
Am J Med Genet 1993 Nov 15;47(7):965-8. doi: 10.1002/ajmg.1320470706. PMID: 7507294

Supplemental Content

Table of contents

    Clinical resources

    Practice guidelines

    • PubMed
      See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.

    Consumer resources

    Reviews

    Related information

    • PubMed
      Related literature resources in PubMed

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...