Hypotrichosis: Causes & Reasons

Possible Causes for Hypotrichosis

WSS should be included in the differential diagnosis of syndromic congenital hypotrichosis. [ncbi.nlm.nih.gov]

Case Report Alopecia and Hypotrichosis as Characteristic Findings in Woodhouse‐Sakati Syndrome: Report of a Family with Mutation in the C2orf37 Gene Regina C. Betz M.D. [doi.org]

Autosomal recessive form of isolated hypotrichosis was identified in six families (AF). [idexlab.com]

Autosomal Recessive Ichthyosis with Hypotrichosis ARCI11

Abstract In this article, we describe a novel autosomal recessive ichthyosis with hypotrichosis syndrome, characterized by congenital ichthyosis associated with abnormal hair [ncbi.nlm.nih.gov]

كلمات كليدي: autosomal recessive congenital ichthyosis, follicular atrophoderma and hypotrichosis, ARCI11 اتوزومال مغلوب ایکتیوز مادرزادی, atrophoderma فولیکولار و hypotrichosis [scipers.com]

[…] and Hypotrichosis that can help you solving undiagnosed cases. [mendelian.co]

Basaran-Yilmaz Syndrome

[…] palmoplantaire Dyskératose Homme Hyperkératose Maladie congénitale Ongle pathologie Peau pathologie Keyword (en) Adult Concomitant disease Child Case study Family study Hypotrichosis [pascal-francis.inist.fr]

A disease characterized by keratoderma, hypotrichosis, and leukonychia totalis. Keratoderma Hypotrichosis Leukonychia Syndrome. [accessanesthesiology.mhmedical.com]

The family presented with congenital hypotrichosis, dry skin, keratosis pilaris, and leukonychia totalis. [accessanesthesiology.mhmedical.com]

Roberts Syndrome

COMPASSIONATE ALLOWANCE INFORMATION ROBERTS SYNDROME ALTERNATE NAMES Roberts Disease; Appelt-Gerken-Lenz Syndrome; Appelt-Gerken-Lenz Disease; Hypomelia Hypotrichosis Facial [secure.ssa.gov]

National Center for Advancing Translational Sciences Home Browse by Disease Roberts Syndrome Roberts Syndrome Other Names: Appelt-Gerken-Lenz syndrome; Hypomelia hypotrichosis [rarediseases.info.nih.gov]

Other Names for This Condition Appelt-Gerken-Lenz syndrome hypomelia hypotrichosis facial hemangioma syndrome pseudothalidomide syndrome RBS Roberts-SC phocomelia syndrome [encyclopedia.pub]

Bjornstad Syndrome

BJORNSTAD PHENOTYPE ASSOCIATED WITH BCS1L MUTATION. 62 Akduman H...Arsan S 30226971 2016 31 Exome sequencing reveals novel BCS1L mutations in siblings with hearing loss and hypotrichosis [malacards.org]

Follicular atrophoderma, multiple basal cell carcinomas and hypotrichosis]. Hautarzt. 1993 Jun;44(6):385-91. [keratin.com]

[…] syndrome (anhidrotic ectodermal dysplasia, cleft lip, cleft palate, hypodontia, nail abnormalities, hypospadias in males); trichodysplasia-xeroderma (skin xerosis, alopecia, hypotrichosis [scielo.br]

Malnutrition

Physical examination findings included generalized nonpitting edema, widespread desquamative plaques, and sparse hair with a reddish tinge. [ncbi.nlm.nih.gov]

hair that falls out easily A tendency to bruise easily Immune system Impaired ability to fight infections and repair wounds If people starve for about 1 month, they lose [merckmanuals.com]

[…] needed substances) Low body temperature (hypothermia) Accumulation of fluid in the arms, legs, and abdomen Disappearance of fat Skin and hair Thin, dry, inelastic skin Dry, sparse [merckmanuals.com]

Zinc Deficiency

Zinc deficiency may manifest as acne, eczema, xerosis (dry, scaling skin), seborrheic dermatitis, or alopecia (thin and sparse hair). [en.wikipedia.org]

Marasmus

Other symptoms include loss of appetite, diarrhea, skin that is dry and baggy, sparse hair that is dull brown or reddish yellow, mental retardation, behavioral retardation [healthofchildren.com]

Body weight is below 60% of that expected for age; the infant looks ‘old’, has thin sparse hair, is pallid and apathetic, lacks skin fat, and has subnormal temperature. [encyclopedia.com]

Panhypopituitarism

She had multiple ecchymoses and sparse hair covering her armpits and eye brows. Her heart rate was 70 beats/min, and her blood pressure was 90/50 mm Hg. [cmaj.ca]

Rombo Syndrome

Abstract This hitherto unknown and dominantly inherited disorder is characterized by vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, basal cell carcinomas [unboundmedicine.com]

Congenital hypotrichosis, eruptive milia, and palmoplantar pits: A case report with review of literature. [ijtrichology.com]

@article{Michalsson1981TheRS, title={The Rombo syndrome: a familial disorder with vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, basal cell carcinomas [semanticscholar.org]

Bazex Syndrome

A Scottish family with Bazex-Dupré-Christol syndrome: follicular atrophoderma, congenital hypotrichosis, and basal cell carcinoma. [unboundmedicine.com]

Hypotrichosis, hypohidrosis, milia and early manifesting basal cell carcinomas. [altmeyers.org]

Congenital hypotrichosis, eruptive milia, and palmoplantar pits: A case report with review of literature. [ijtrichology.com]

Hallermann-Streiff Syndrome

Abstract The Hallermann-Streiff syndrome is characterized by dyscephaly, hypotrichosis, microphthalmia, cataracts, beaked nose, micrognathia, and proportionate short stature [unboundmedicine.com]

Figure 1: Natal teeth, parrot beaked nose, micrognathia, atrophic skin, hypotrichosis. [pediatriconcall.com]

Hallermann-Streiff syndrome-also called occulomandibulofacial syndrome, Francois syndrome, oculomandibulodyscephaly with hypotrichosis, Aubry syndrome I, and Ullrich-Fremery-Dohna [ncbi.nlm.nih.gov]

Hidrotic Ectodermal Dysplasia

The phenotype in this family ranged from atrichosis to hypotrichosis, sparsity or absence of eyebrows, and thickening of palms and soles. [ncbi.nlm.nih.gov]

The presence of nail abnormalities with hypotrichosis also separates our case from various forms of atrichia congenita or congenital hypotrichosis. [ijpd.in]

HED is characterized by lack of or diminished sweating (anhidrosis or hypohidrosis), abnormally sparse hair (hypotrichosis), and/or absence (hypodontia) and/or malformation [rarediseases.org]

Diffuse Palmoplantar Keratoderma

However, universal hypotrichosis and the lack of oral leukokeratosis were the differentiating features in our case. [ncbi.nlm.nih.gov]

Diffuse palmoplantar keratoderma, onychodystrophy, universal hypotrichosis and cysts Abstract No abstract available References References: Asai Y & Irvine AD. [adc.mef.hr]

[…] include Howel–Evans syndrome (focal keratoderma on pressure sites, leukokeratosis of the oral mucosa and esophageal cancer); Clouston syndrome (hidrotic ectodermal dysplasia, hypotrichosis [indianpediatrics.net]

Chronic Hepatitis

Clin Exp Med. 2018 Aug;18(3):433-443. doi: 10.1007/s10238-018-0501-x. Epub 2018 Apr 25. Wu SD 1, 2, Liu LL 1, 2, Cheng JL 3, Liu Y 1, Cheng LS 1, Wang SQ 1, Ma W 1, Chen LP 3, Tseng YJ 1, Wang JY 1, 2, Shen XZ 1, 2, Jiang W 4, 5. Author information 1 Department of Gastroenterology and Hepatology, Zhongshan Hospital, Fudan[…] [ncbi.nlm.nih.gov]

Oculodentodigital Dysplasia

[…] facies, ocular findings (microphthalmia, microcornea, glaucoma), syndactyly type III of the hands, phalangeal abnormalities, diffuse skeletal dysplasia, enamel dysplasia, and hypotrichosis [ncbi.nlm.nih.gov]

Less common features include hypotrichosis, intracranial calcifications, and conductive deafness secondary to recurrent otitis media. [ncbi.nlm.nih.gov]

In some types, teeth may be missing and nails may be defective, while in another type there may be missing teeth, inability to sweat, and sparse hair. [nfed.org]

Melhem-Fahl Syndrome

Lagoyanni syndrome Kennerknecht Sorgo Oberhoffer syndrome Kennerknecht Vogel syndrome Kenny Caffey syndrome Kenny-Caffey syndrome, Type 1 Keratitis, hereditary Keratoderma hypotrichosis [en.wikipedia.org]

Syndrome + Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome Ichthyosis Cheek Eyebrow Syndrome Ichthyosis Follicularis Atrichia Photophobia Syndrome [rgd.mcw.edu]

Mari type Marie Unna congenital hypotrichosis Marie Unna hereditary hypotrichosis - See Marie Unna congenital hypotrichosis Marie-Sainton disease - See Cleidocranial dysplasia [herenciageneticayenfermedad.blogspot.com]

Granulomatous Hepatitis

Intravesical bacillus Calmette-Guerin (BCG) is used in patients with urinary bladder carcinoma. Although it is generally well tolerated, granulomatous hepatitis is a rare but serious complication. We report a 42-year-old man and a 56-year-old man who developed granulomatous hepatitis following intravesical BCG. One of[…] [ncbi.nlm.nih.gov]

Wiedemann-Rautenstrauch Syndrome

[…] to navigation Jump to search Wiedemann-Rautenstrauch syndrome is a very rare disorder with features of premature aging recognizable at birth, decreased subcutaneous fat, hypotrichosis [wikidata.org]

Hypotrichosis Marked hypotrichosis, Hypotrichosis, infantile, Congenital hypotrichosis [more] Congenital lack of hair growth. [rarediseases.oscar.ncsu.edu]

Wiedemann-Rautenstrauch syndrome Wiedemann-Rautenstrauch syndrome is a very rare disorder with features of premature aging recognizable at birth, decreased subcutaneous fat, hypotrichosis [wikidata.org]

Hypergonadotropic Hypogonadism - Partial Alopecia

Familial juvenile macular dystrophy with congenital hypotrichosis capitis. Ophthalmology 1998;95:233–240. CrossRef Google Scholar 16. [link.springer.com]

Hypotrichosis Simplex Hypotrichosis Simplex of Scalp Hypoxanthine Guanine Phosphoribosyltransferase Deficiency Hystrix-Like Ichthyosis with Deafness, Keratitis-ichthyosis-deafness [sequencing.com]

[…] mental retardation Lopes type Hypotrichosis Hypotropia Hypoxanthine guanine phosphoribosyltransferase deficiency Hypoxia Advertisements [thefullwiki.org]

Palmoplantar Keratosis

As a result, they have cystic nodules on the eyelids, thickening of the skin on the palms of the hands and soles of the feet, missing teeth, sparse hair, and underdeveloped [nutritionhouse.com]

Keratosis palmoplantaris striata 1 31,329,949(+) A/T coding_sequence_variant, stop_gained rs398122400 pathogenic, Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis [genecards.org]

Keywords: Genodermatosis, hypotrichosis, Olmsted syndrome, onychodystrophy, palmoplantar keratoderma How to cite this article: Kumar P, Sharma P K, Kar H K. [doi.org]

Ectodermal Dysplasia

We propose a combination of topical cetirizine and oral vitamin D as a rational treatment of choice in congenital hypotrichosis caused by ectodermal dysplasia. [ncbi.nlm.nih.gov]

Odonto-onycho-dermal dysplasia (OODD) is a rare form of ectodermal dysplasia characterized by severe oligodontia, onychodysplasia, palmoplantar hyperkeratosis, dry skin, hypotrichosis [ncbi.nlm.nih.gov]

Depending on the variety, hypohidrosis, hypotrichosis, hypodontia, oligodontia, and/or anodontia may be exhibited. Few long-term clinical reports exist. [ncbi.nlm.nih.gov]

Kwashiorkor

hair that falls out easily A tendency to bruise easily Immune system Impaired ability to fight infections and repair wounds If people starve for about 1 month, they lose [merckmanuals.com]

Four patients had noticeably sparse hair, and 1 had mild depigmentation of his hair for the 3 months before presentation. [jamanetwork.com]

Cartilage Hair Hypoplasia

We present a series of six patients with the same radiological changes, but without apparent hypotrichosis. [ncbi.nlm.nih.gov]

We conclude that recessive metaphyseal dysplasia without hypotrichosis is a variant of CHH, manifesting only as short stature and metaphyseal dysplasia. [ncbi.nlm.nih.gov]

Cartilage-hair hypoplasia is an autosomal recessive disorder, characterized by short stature, metaphyseal dysplasia, hypotrichosis and immunodeficiency. [ncbi.nlm.nih.gov]

Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

1 hypotrichosis 10 hypotrichosis 11 hypotrichosis 12 hypotrichosis 13 hypotrichosis 2 hypotrichosis 3 hypotrichosis 4 hypotrichosis 5 hypotrichosis 6 hypotrichosis 7 hypotrichosis [rgd.mcw.edu]

Basaran Yilmaz syndrome 0 *Hypotrichosis *Keratoderma, Palmoplantar *Nail Diseases *Pigmentation Disorders. Hypotrichosis simplex 0 *Hypotrichosis. [reference.md]

An unknown spondyloepimetaphyseal dysplasia with a positive sweat chloride test, sparse hair and mild facial dysmorphism. Clin. Dysmorph. 3: 309-317, 1994. [omim.org]

Anauxetic Dysplasia

Called also alopecia. canine hereditary hypotrichosis congenital hypotrichosis absence of hair at birth. [medical-dictionary.thefreedictionary.com]

Entry H00518 Disease Name Metaphyseal dysplasia without hypotrichosis Supergrp Metaphyseal dysplasias [DS: H00479 ] Description Metaphyseal dysplasia without hypotrichosis [genome.jp]

Metaphyseal dysplasia without hypotrichosis was initially described as a distinct entity from CHH with identical skeletal features, and lacking hypotrichosis and immunodeficiency [genedx.com]

Autosomal Recessive Primary Microcephaly Type 10

And Recurrent Skin Vesicles DSC3 Hypotrichosis-Lymphedema-Telangiectasia Syndrome SOX18 Hypoxia-Ischemia, Brain VEGFA Immunologic Deficiency Syndromes C5 Intestinal Neoplasms [selfdecode.com]

1,605389 CDSN Hypotrichosis 2,146520 KRT74 Hypotrichosis 3,613981 HR Hypotrichosis 4,146550 DSG4 Hypotrichosis 6,607903 LIPH Hypotrichosis 7,604379 LPAR6 Hypotrichosis 8,278150 [gsdseq.ir]

[…] genetic alterations Brachydactyly and Lymphoma, related diseases and genetic alterations Tremor and Short neck, related diseases and genetic alterations High palate and Hypotrichosis [mendelian.co]

Hirschsprung Disease Type D-Brachydactyly Syndrome

[…] mental retardation Lopes type Hypotrichosis Hypotropia Hypoxanthine guanine phosphoribosyltransferase deficiency Hypoxia [wikidoc.org]

INPP5E Mental retardation, X-linked syndromic, Turner type HUWE1 Metaphyseal anadysplasia type 1 MMP13 Metaphyseal anadysplasia type 2 MMP9 Metaphyseal dysplasia without hypotrichosis [centogene.com]

Atrichia with Papular Lesions

among many others, can involve the symptom of hypotrichosis. [webmd.com]

Mutations in this upstream ORF cause Marie Unna hereditary hypotrichosis (MUHH), an autosomal dominant form of genetic hair loss. [genecards.org]

A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2). [jpma.org.pk]

Oculo-Osteo-Cutaneous Syndrome

Symptoms - Brachymetapody anodontia hypotrichosis albinoidism Causes - Brachymetapody anodontia hypotrichosis albinoidism Not supplied. [checkorphan.org]

Brachymetapody-Anodontia-Hypotrichosis Albinoidism Syndrome (Anodontia-Hypotrichosis Syndrome) &nb 515c27f sp; &nb 515c27f sp; &nb 515c27f sp; &nb 515c27f sp; &nb 515c27f [esanatos.com]