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Abnormal hair pattern

MedGen UID:
869295
•Concept ID:
C4023721
•
Finding
Synonym: Abnormal hair patterning
 
HPO: HP:0010720

Definition

An abnormality of the distribution of hair growth. [from HPO]

Professional guidelines

PubMed

Corticosteroids for the treatment of Duchenne muscular dystrophy.
Matthews E, Brassington R, Kuntzer T, Jichi F, Manzur AY
Cochrane Database Syst Rev 2016 May 5;2016(5):CD003725. doi: 10.1002/14651858.CD003725.pub4. PMID: 27149418Free PMC Article
AMERICAN ASSOCIATION OF CLINICAL ENDOCRINOLOGISTS, AMERICAN COLLEGE OF ENDOCRINOLOGY, AND ANDROGEN EXCESS AND PCOS SOCIETY DISEASE STATE CLINICAL REVIEW: GUIDE TO THE BEST PRACTICES IN THE EVALUATION AND TREATMENT OF POLYCYSTIC OVARY SYNDROME--PART 1.
Goodman NF, Cobin RH, Futterweit W, Glueck JS, Legro RS, Carmina E; American Association of Clinical Endocrinologists (AACE); American College of Endocrinology (ACE); Androgen Excess and PCOS Society (AES)
Endocr Pract 2015 Nov;21(11):1291-300. doi: 10.4158/EP15748.DSC. PMID: 26509855
Hirsutism: diagnosis and treatment.
Hohl A, Ronsoni MF, Oliveira Md
Arq Bras Endocrinol Metabol 2014 Mar;58(2):97-107. doi: 10.1590/0004-2730000002923. PMID: 24830586

Recent clinical studies

Diagnosis

Two novel UBR1 gene mutations ın a patient with Johanson Blizzard Syndrome: A mild phenotype without mental retardation.
Atik T, Karakoyun M, Sukalo M, Zenker M, Ozkinay F, Aydoğdu S
Gene 2015 Oct 1;570(1):153-5. Epub 2015 Jul 3 doi: 10.1016/j.gene.2015.06.082. PMID: 26149651
Oligohydramnios sequence revisited in relationship to arthrogryposis, with distinctive skin changes.
Hall JG
Am J Med Genet A 2014 Nov;164A(11):2775-92. Epub 2014 Aug 26 doi: 10.1002/ajmg.a.36731. PMID: 25160497
Brown-Vialetto-van Laere syndrome: a riboflavin responsive neuronopathy of infancy with singular features.
Spagnoli C, Pitt MC, Rahman S, de Sousa C
Eur J Paediatr Neurol 2014 Mar;18(2):231-4. Epub 2013 Oct 16 doi: 10.1016/j.ejpn.2013.09.006. PMID: 24206674

Therapy

Brown-Vialetto-van Laere syndrome: a riboflavin responsive neuronopathy of infancy with singular features.
Spagnoli C, Pitt MC, Rahman S, de Sousa C
Eur J Paediatr Neurol 2014 Mar;18(2):231-4. Epub 2013 Oct 16 doi: 10.1016/j.ejpn.2013.09.006. PMID: 24206674

Clinical prediction guides

Oligohydramnios sequence revisited in relationship to arthrogryposis, with distinctive skin changes.
Hall JG
Am J Med Genet A 2014 Nov;164A(11):2775-92. Epub 2014 Aug 26 doi: 10.1002/ajmg.a.36731. PMID: 25160497
Brown-Vialetto-van Laere syndrome: a riboflavin responsive neuronopathy of infancy with singular features.
Spagnoli C, Pitt MC, Rahman S, de Sousa C
Eur J Paediatr Neurol 2014 Mar;18(2):231-4. Epub 2013 Oct 16 doi: 10.1016/j.ejpn.2013.09.006. PMID: 24206674

Supplemental Content

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