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23 Possible Causes for Congenital Alopecia, Facial Hemiatrophy, Hypopituitarism

  • 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] Digitorenocerebral Syndrome Dincsoy Salih Patel Syndrome Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation Distal Arthrogryposis, with Hypopituitarism[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] Primary growth hormone (GH) deficiency was ruled out in all patients, although one of them might have developed secondary GH deficiency due to partial hypopituitarism following[ncbi.nlm.nih.gov] alopecia of a zone of the occipital and posterior parietal scalp is presented.[ncbi.nlm.nih.gov]

  • Alopecia

    Endocrinopathies Diabetes Hypothyroidism Hypopituitarism Nutritional disorders Hypervitaminosis A Zinc deficiency (eg, Acrodermatitis enteropathica) Iron deficiency Marasmus[pedclerk.bsd.uchicago.edu] Congenital triangular alopecia Congenital triangular alopecia references Congenital triangular alopecia Congenital triangular alopecia is a patch of hair loss in the temple[keratin.com] Despite the low prevalence, congenital alopecia areata is an important differential diagnosis for neonatal hair loss.[ncbi.nlm.nih.gov]

  • Salti-Salem Syndrome

    hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder Failed Back Surgery Syndrome Familial Antiphospholipid[rgd.mcw.edu] Hypopituitarism and septooptic 'dysplasia' - See Septo-optic dysplasia spectrum Hypoplasia hepatic ductular Hypoplasia of the right ventricle - See Right ventricle hypoplasia[herenciageneticayenfermedad.blogspot.com] Alopecia X-Linked Congenital Infantile Muscular Dystrophy with Cataract and Hypogonadism Cutaneous Telangiectasia and Cancer Syndrome, Familial De Sanctis-Cacchione Syndrome[rgd.mcw.edu]

  • Chudley-Rozdilsky Syndrome

    Abnormalities, Kyphoscoliosis, and Mental Retardation Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, and Gingival Overgrowth Syndrome facial[rgd.mcw.edu] With this… Hypopituitarism affects many children with cerebral palsy. The condition causes poor growth, often delaying puberty.[patientworthy.com] […] absence of the sternocleidomastoid muscle Congenital adrenal hyperplasia Congenital alopecia X-linked Congenital amegakaryocytic thrombocytopenia Congenital amputation Congenital[personalizedcause.com]

  • Skin Atrophy

    hemiatrophy.[blackwellreference.com] Image courtesy of the National Institute on Aging/National Institutes of Health Simmonds disease is a chronic deficiency of function of the pituitary gland, a form of hypopituitarism[britannica.com] Scarring alopecia, congenital absence of three toenails, and a scarlike lesion of the tongue were also present.[ncbi.nlm.nih.gov]

  • 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] C 3/4 CHIME syndrome - See Zunich neuroectodermal syndrome Chitayat Meunier Hodgkinson syndrome Chitayat-Hall syndrome - See Distal arthrogryposis with hypopituitarism, intellectual[herenciageneticayenfermedad.blogspot.com] Azathioprine: Corticosteroid sparing agent Scleroderma Types Localized scleroderma Morphea: Plaques of skin fibrosis Linear scleroderma: Bands of fibrosis; May be associated with facial[neuromuscular.wustl.edu]

  • Craniorhiny

    FACIAL HEMIATROPHY  Atrophy of the soft tissues of half of the face i.e skin, muscles, bones, soft palate. 37 38.[slideshare.net] ALAZAMI-YUAN SYNDROME Alopecia, epilepsy, pyorrhea, mental subnormality Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Arthrogryposis, distal, with hypopituitarism[ctdbase.org] ; CCCA OMIM:217600 Central Cloudy Dystrophy of Francois; CCDF OMIM:117000 Central Core Disease of Muscle; CCD OMIM:209880 Central Hypoventilation Syndrome, Congenital; CCHS[informatics.jax.org]

  • Autosomal Recessive Spastic Ataxia with Leukoencephalopathy

    543 2 瘢痕回(ulegyria) 544 6 側頭脳瘤(temporal encephalocele) 545 7 Rasmussen脳炎(Rasmussen's encephalitis) 546 8 神経節膠腫(ganglioglioma) 549 9 Parry-Romberg症候群(進行性顔面片側萎縮症progressive facial[rnavi.ndl.go.jp] Charcot-Marie-Tooth disease Charcot-Marie-Tooth disease - deafness - intellectual disability Childhood apraxia of speech Childhood-onset hypophosphatasia Chilblain lupus Choroidermia - hypopituitarism[sanfordresearch.org] […] androgenic alopecia, see androgenetic alopecia ANE1, see acute necrotizing encephalopathy type 1 Anemia, Dyserythropoietic, Congenital, see congenital dyserythropoietic anemia[mygenomics.com]

  • Autosomal Recessive Spastic Paraplegia Type 14

    543 2 瘢痕回(ulegyria) 544 6 側頭脳瘤(temporal encephalocele) 545 7 Rasmussen脳炎(Rasmussen's encephalitis) 546 8 神経節膠腫(ganglioglioma) 549 9 Parry-Romberg症候群(進行性顔面片側萎縮症progressive facial[rnavi.ndl.go.jp] […] syndrome Recurrent hydatidiform mole 1 Recurrent hydatidiform mole 2 Reduced response to beta-2-adrenoreceptor agonist Renal cysts and diabetes (RCAD) Renal dysplasia with hypopituitarism[moldiag.com] Genetic Testing - T cell immunodeficiency, congenital alopecia and nail dystrophy (T-cell immunodeficiency, congenital alopecia and nail dystrophy) - Gen FOXN1.[ivami.com]

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