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78 Possible Causes for Congenital Alopecia, Facial Hemiatrophy, Short Bowel Syndrome

  • Tollner-Horst-Manzke Syndrome

    Abnormalities, Kyphoscoliosis, and Mental Retardation Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, and Gingival Overgrowth Syndrome facial[rgd.mcw.edu] alopecia Autosomal dominant partial epilepsy with auditory features Autosomal dominant polycystic kidney disease - Not a rare disease Autosomal dominant pseudohypoaldosteronism[rarediseases.info.nih.gov] Ramji Syndrome SHASHI-PENA SYNDROME Sheehan syndrome short bowel syndrome short QT syndrome SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES[rgd.mcw.edu]

  • Cerebellotrigeminal Dermal Dysplasia

    hemiatrophy (Parry-Romberg syndrome) Linear scleroderma (morphoea) en coup de sabre Unilateral somatic and intracranial hypoplasia Oculocerebrocutaneous syndrome (Delleman[chipsbooks.com] alopecia of a zone of the occipital and posterior parietal scalp is presented.[ncbi.nlm.nih.gov] bowel syndrome).[sites.uclouvain.be]

  • Salti-Salem Syndrome

    hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder Failed Back Surgery Syndrome Familial Antiphospholipid[rgd.mcw.edu] Alopecia X-Linked Congenital Infantile Muscular Dystrophy with Cataract and Hypogonadism Cutaneous Telangiectasia and Cancer Syndrome, Familial De Sanctis-Cacchione Syndrome[rgd.mcw.edu] Sho [ edit ] Shock Shokeir syndrome Shor [ edit ] Short b – Short r [ edit ] Short bowel syndrome Short broad great toe macrocranium Short-chain acyl-CoA dehydrogenase deficiency[en.wikipedia.org]

  • FLOTCH Syndrome

    hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder Failed Back Surgery Syndrome Familial Antiphospholipid[rgd.mcw.edu] Ann Dermatol Venereol. 1986;113(6-7):549-53 T- cell immunodeficiency, congenital alopecia and nail dystrophy 0 *Alopecia *Nail Diseases *Severe Combined Immunodeficiency.[reference.md] Home Short Bowel Syndrome Image ID: 6718 , Reg ID: i6495 Please describe![netterimages.com]

  • Phakomatosis Pigmentokeratotica

    Pascual-Castroviejo Progressive facial hemiatrophy I. Pascual-Castroviejo Unilateral facial and intracranial hypoplasia[hoepli.it] Alopecia Syndrome Other Disorders of Keratinization Porokeratoses Kyrle’s Disease Pityriasis Rubra Pilaris Poikilodermas and Aging Syndromes Disorders of DNA Repair Aging[routledge.com] Sho Shok • Shor • Shou Shock Shok Shokeir syndrome Shor Short b – Short r Short bowel syndrome Short broad great toe macrocranium Short-chain acyl-CoA dehydrogenase deficiency[sosu.us]

  • Chudley-Rozdilsky Syndrome

    Abnormalities, Kyphoscoliosis, and Mental Retardation Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, and Gingival Overgrowth Syndrome facial[rgd.mcw.edu] […] absence of the sternocleidomastoid muscle Congenital adrenal hyperplasia Congenital alopecia X-linked Congenital amegakaryocytic thrombocytopenia Congenital amputation Congenital[personalizedcause.com] Among the maladies of… Short bowel syndrome, which is also called short gut, occurs as a result of someone having at least half of their small intestine removed, and sometimes[dev.pworthy.webfactional.com]

  • Congenital Trigeminal Anesthesia

    Masticatory spasm in facial hemiatrophy. Ann Neurol 1980;7:585–587. 52. Kim JS, Choi-Kwon S. Sensory sequelae of medullary infarction.[neupsykey.com] Giant congenital triangular alopecia mimicking alopecia areata.[ijtrichology.com] ) CROME Congenital Cataracts-epileptic Fits-mental Retardation [syndrome] CRS Congenital Rubella Syndrome CS Congenital Syphilis CSB Congenital Short Bowel CSHH Congenital[medicabbreviations.com]

  • Schwartz-Lelek Syndrome

    hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder Failed Back Surgery Syndrome Familial Antiphospholipid[rgd.mcw.edu] ALOPECIA 1[panelapp.genomicsengland.co.uk] bowel syndrome Congenital stromal corneal dystrophy Congenital valvular dysplasia Distal myopathy with posterior leg and anterior hand involvement Ehlers-Danlos syndrome[csbg.cnb.csic.es]

  • CANOMAD Syndrome

    hemiatrophy En coup de sabre Systemic sclerosis (Scleroderma): Subtypes Diffuse cutaneous scleroderma Rapidly progressive Widespread skin thickening Similar syndromes 2 toxins[neuromuscular.wustl.edu] […] absence adrenal alopecia amegakaryocytic aneurysms great antithrombin aplastic arteriovenous shuntCongenital benign spinal muscular atrophy bilateral bronchobiliary cardiovascular[shecandothat.net] Shaken Baby Syndrome Shapiro Syndrome Sharma Kapoor Ramji Syndrome SHASHI-PENA SYNDROME Sheehan syndrome short bowel syndrome short QT syndrome SHORT STATURE WITH MICROCEPHALY[rgd.mcw.edu]

  • Hallermann-Streiff Syndrome

    hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder Failed Back Surgery Syndrome Familial Antiphospholipid[rgd.mcw.edu] Synonym: congenital sutural alopecia, hallermann-streiff syndrome, hallermann-streiff-francois syndrome, mandibulo-oculofacial syndrome, oculomandibulodyscephaly, oculomandibulofacial[biology-online.org] Alopecia 2 Palmoplantar Keratoderma and Congenital Alopecia, Autosomal Dominant Papillon-Lefevre Syndrome Pili Torti and Developmental Delay Pilodental Dysplasia with Refractive[nfed.org]

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