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792 Possible Causes for Alopecia, prenatal and postnatal, Short Stature

  • Wiedemann-Rautenstrauch Syndrome

    Patients have premature aging aspect, short stature and a poorly muscled build.[] She had prenatal and postnatal growth failure, generalized lipoatrophy except for fat pads in the suprabuttock areas, triangular face, pseudohydrocephalous, sparse scalp hair[] Prominent scalp veins are noticeable (made more obvious by alopecia), as well as prominent eyes.[]

  • Turner Syndrome

    stature (Short-Stature Group) were enrolled.[] Research Prenatal and postnatal...[] An association with many autoimmune diseases is described as well as skin diseases such as psoriasis, vitiligo and alopecia areata.[]

  • Seckel Syndrome

    Seckel syndrome is a very rare form of primordial dwarfism characterized by antenatal and postnatal growth delay, proportionate extreme short stature, a prominent beak-like[] Abstract BACKGROUND Primordial dwarfism (PD) is an extremely rare, clinicallyheterogeneous condition characterised by profound prenatal and postnatal growth restriction among[] Affected individuals displayed telangiectases, alopecia, and other malignancies such as nonmelanoma skin cancer, and less commonly breast cancer and cervical cancer.[]

  • Klinefelter Syndrome

    We present a patient with Klinefelter syndrome and short stature due to growth hormone deficiency.[] The objective of this study was to describe the prevalence of Klinefelter syndrome (KS) prenatally and postnatally in Denmark and determine the influence of maternal age.[] These patients usually present with tall stature. We report a case of KS with short stature due to growth hormone deficiency.[]

  • Rothmund Thomson Syndrome

    Targeted next-generation sequencing (NGS) using a custom panel consisting of 705 short-stature-related genes was performed for the probands.[] Growth and development: A large percentage of individuals with RTS experience abnormally slow growth before and after birth (prenatal and postnatal growth retardation), leading[] A 20-year-old male developed early blistering, poikiloderma, hypohidrosis, alopecia and exocrine pancreatic hypofunction caused by atrophy and fatty replacement of the pancreas[]

  • Chondrodysplasia Punctata

    A subtype of CDP, X-linked dominant chondrodysplasia punctata (CDPX2), known also as Conradi-Hünermann-Happle syndrome, is a rare skeletal dysplasia characterized by short[] We report the prenatal management of a brachytelephalangic chondrodysplasia punctata (CDPX1) case and how postnatal findings confirmed the diagnosis.[] A 5-year-old girl presented for evaluation of ill-defined patches of cicatricial alopecia.[]

  • Laron Syndrome

    It is sometimes classified as either proportional short stature or dysproportional short stature such as cases of achodroplasia, hypochondroplasia and multiple epiphyseal[] Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study. J Clin Endocrinol Metab 2003;88:622-6. Nielsen J, Wohlert M.[] Young adults have various degrees of alopecia, more pronounced in males.[]

  • Sanjad-Sakati Syndrome

    Sanjad Sakati Syndrome /Dysmorphism/ short stature 30 Days of Hope: Day Nine #NICUphotography, #preemie, #NICU, #placentaprevia, #34weeks, #preemiesupportandawareness, #capturinghopes[] It is characterized by congenital hypoparathyroidism, severe prenatal and postnatal growth retardation, and distinct facial dysmorphism.[] Synonym(s): Sakati-Nyhan syndrome Sakati-Nyhan syndrome - rare syndrome, usually sporadic, featuring craniofacial defects, abnormal limbs, congenital heart defects, patchy alopecia[]

  • Ichthyosis and Male Hypogonadism

    stature Long thin fingers Absent eyebrows Sparse eyebrows Glaucoma Undescended testes Small penis Hypothyroidy Small teeth Peripheral retinal pigmentary changes Sparse scalp[] STS deficiency may be readily diagnosed either prenatally or postnatally by a combination of enzymatic, endocrinologic, and molecular methods.[] الصفحة 38 - Changes in hair weight and hair count in men with androgenetic alopecia, after application of 5% and 2% topical minoxidil, placebo, or no treatment.[]

  • Menkes Disease

    stature, facial Multiple malformation syndrome, small stature, without skeletal dysplasia MVRCS association Nail-patella syndrome Nance-Horan syndrome Neu-Laxova syndrome[] PubMed Central View Article PubMed Google Scholar Tønnesen T, Horn N: Prenatal and postnatal diagnosis of Menkes disease, an inherited disorder of copper metabolism.[] […] torti : Bjornstad syndrome Crandall syndrome Mitochondrial disorders Netherton syndrome Bazex-Dupré-Christol syndrome Citrullinemia Laron syndrome Child abuse (eg, traumatic alopecia[]

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