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Absent eyebrow
Known as:
Missing eyebrows
, Eyebrows absent
, Failure of development of eyebrows
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Absence of the eyebrow. [HPO:probinson]
National Institutes of Health
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Related topics
Related topics
6 relations
ABLEPHARON-MACROSTOMIA SYNDROME
Arthrogryposis and ectodermal dysplasia
Glomerulonephritis sparse hair telangiectases
HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME
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Narrower (1)
Madarosis of eyebrow
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
In Silico Analysis of Missense Mutations in LPAR6 Reveals Abnormal Phospholipid Signaling Pathway Leading to Hypotrichosis
S. I. Raza
,
D. Muhammad
,
+4 authors
Sajid Rashid
PLoS ONE
2014
Corpus ID: 7583936
Autosomal recessive hypotrichosis is a rare genetic irreversible hair loss disorder characterized by sparse scalp hair, sparse to…
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2014
2014
Effect of eyes and eyebrows on face recognition system performance
Nadjet Radji
,
D. Cherifi
,
A. Azrar
International Image Processing, Applications and…
2014
Corpus ID: 18306722
In this paper, we evaluate the effect of removing eyes or eyebrows from face image (no left eyebrow, no right eyebrow, no…
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2013
2013
A novel mutation, c.699C>G (p.C233W), in the LIPH gene leads to a loss of the hydrolytic activity and the LPA6 activation ability of PA-PLA1α in autosomal recessive wooly hair/hypotrichosis.
M. Yoshizawa
,
Motonobu Nakamura
,
M. Farooq
,
A. Inoue
,
J. Aoki
,
Y. Shimomura
Journal of dermatological science (Amsterdam)
2013
Corpus ID: 5516987
Review
2013
Review
2013
Ulerythema Ophryogenes, A Rarely Reported Cutaneous Manifestation of Noonan Syndrome: Case Report and Review of the Literature
Kayi Li
,
Mary Thomas
,
R. Haber
Journal of Cutaneous Medicine and Surgery
2013
Corpus ID: 8466331
Background: Ulerythema ophryogenes (also known as keratosis pilaris atrophicans faciei) is a rarely reported cutaneous…
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2011
2011
Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan
S. Khan
,
R. Habib
,
+13 authors
W. Ahmad
Clincal and Experimental Dermatology
2011
Corpus ID: 20008568
Background. Autosomal recessive hypotrichosis/woolly hair is a rare genetic hair loss disorder characterized by sparse scalp…
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2009
2009
Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families
M. Tariq
,
M. Ayub
,
+12 authors
W. Ahmad
British Journal of Dermatology
2009
Corpus ID: 26858830
Background Autosomal recessive hypotrichosis is a rare genetic irreversible hair loss characterized by sparse scalp hair, sparse…
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2007
2007
Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11–q21.32
A. Wali
,
M. Chishti
,
+5 authors
Wasim Ahmad
Clinical Genetics
2007
Corpus ID: 1739094
Autosomal recessive hypotrichosis is a rare form of alopecia characterized by sparse hair on scalp, sparse to absent eyebrows and…
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1991
1991
A distinct type of hidrotic ectodermal dysplasia.
F. Halal
,
N. Setton
,
N. Wang
American journal of medical genetics
1991
Corpus ID: 33722205
Four individuals from 2 generations of a family had a hidrotic type of ectodermal dysplasia (ED). Males and females were…
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1979
1979
Burn injuries of the eyelids.
T. Huang
,
S. Blackwell
,
S. R. Lewis
Clinics in Plastic Surgery
1979
Corpus ID: 39574572
Burns of the eyelid and surrounding structures are relatively uncommon in spite of a high incidence of thermal injuries involving…
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1978
1978
Burn Injuries of the Eyelids
Ted T. Huang
,
S. Blackwell
,
S. R. Lewis
1978
Corpus ID: 227312651
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