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45 Possible Causes for Congenital Alopecia, Sheehan Syndrome, Zinc Deficiency

  • Hypothyroidism

    […] of the puppy coat, hyperpigmentation of the skin, and bilaterally symmetric alopecia of the trunk.[] While zinc deficiency is very uncommon in the developed world, it’s still recommended to eat a variety of zinc-rich foods ( 8 ).[] Sheehan Syndrome Sheehan syndrome, a postpartum complication in which pituitary cells are infarcted due to increased blood loss during delivery may lead to decreased production[]

  • Erythroderma Desquamativum

    Alopecia and Nail Dystrophy *601863 Regulatory Factor 5; RFX5 *602450 Severe Combined Immunodeficiency, Athabascan Type; SCIDA *602667 Nijmegen Breakage Syndrome Gene; NBS1[] […] enzyme that may serve as surrogate diagnostic marker of zinc deficiency.[] Setleis Syndrome Severe Combined Immunodeficiency Sheehan syndrome Short Bowel Syndrome Short Chain Acyl CoA Dehydrogenase Deficiency (SCAD) SHORT Syndrome Shwachman Syndrome[]

  • Laron Syndrome with Immunodeficiency

    alopecia and nail dystrophy H00721 Pyogenic bacterial infections, recurrent, due to MYD88 deficiency [PATH: hsa04210 hsa04620 ] H01240 Immune thrombocytopenia [PATH: hsa04145[] Lorain-Levi short stature Necrosis of pituitary gland (postpartum) Panhypopituitarism Pituitary: · cachexia · insufficiency NOS · short stature Sheehan's syndrome Simmonds[] Lorain-Levi short stature Necrosis of pituitary gland (postpartum) Panhypopituitarism Pituitary cachexia Pituitary insufficiency NOS Pituitary short stature Sheehan's syndrome[]

  • Secondary Hypothyroidism

    Alopecia, weight gain, mental dullness, fatigue, cold intolerance, infertility and neurological deficits are seen.[] Some of the common ingredients include: Kelp and other products that are sources of iodine; however, iodine deficiency isn’t an issue for most.[] This is a condition known as "Sheehan Syndrome" Infection of the pituitary gland More rarely, certain viral illnesses can cause damage to the pituitary gland either through[]

  • Hereditary Mucoepithelial Dysplasia

    IFAP syndrome is caused by deficiency in MBTPS2, an intramembrane zinc metalloprotease essential for cholesterol homeostasis and ER stress response.[] Congenital alopecia involving the scalp, eyebrows and eyelashes is another essential cutaneous manifestation of IFAP (Figure 1A ).[] Still further contemplated conditions include of endocrinological disorders such as disorders associated with hypopituitarismn including hypogonadism, Sheehan syndrome, diabetes[]

  • Hereditary Hyperekplexia

    […] variant) FOXI1 (Enlarged vestibular aqueduct) FOXL2 (Blepharophimosis, epicanthus inversus, and ptosis, type 1) FOXN1 (T-cell immunodeficiency, congenital alopecia, and nail[] Reduced zinc in breast milk Glutamine deficiency, congenital Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma Oculocutaneous albinism type 3 Type 3 oculocutaneous[] Sharma Kapoor Ramji Syndrome SHASHI-PENA SYNDROME Sheehan syndrome short bowel syndrome short QT syndrome Short Stature-Obesity Syndrome SHORT Syndrome shoulder impingement[]

  • Gorlin-Chaudhry-Moss Syndrome

    Alopecia 2 Palmoplantar Keratoderma and Congenital Alopecia, Autosomal Dominant Papillon-Lefevre Syndrome Pili Torti and Developmental Delay Pilodental Dysplasia with Refractive[] Deficiency due to Low Breast Milk Zinc NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH Neurofaciodigitorenal Syndrome Nijmegen Breakage Syndrome-Like Disorder[] Sennetsu Fever Septo Optic Dysplasia Setleis Syndrome Severe Combined Immunodeficiency Sheehan Syndrome Short Chain Acyl CoA Dehydrogenase Deficiency (SCAD) SHORT Syndrome[]

  • Hypergonadotropic Hypogonadism-Cataract Syndrome

    […] megalocornea Stickler syndrome, type 2 Pitt-Hopkins syndrome Alopecia macular degeneration growth retardation Glycogen storage disease type 5 Hyperlipoproteinemia type 5[] Zinc deficiency is associated with ANEMIA, short stature, HYPOGONADISM, impaired WOUND HEALING, and geophagia. It is known by the symbol Zn.[] […] polycystic ovaries Hypogonadotropic Amyloidosis, Carpenter syndome, fertile eunuch syndrome, Fröhlich syndrome, Sheehan syndrome, Kallmann's disease, Laurence-Moon-Biedl[]

  • Amelo-Onycho-Hypohidrotic Syndrome

    alopecia [ ] Autosomal dominant periodic fever [ ] Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis [ ] Autosomal dominant popliteal pterygium[] , Sheehan Syndrome Environmental Cold weather, Environmental allergen, Excessive swimming in chlorinated pool, Heatstroke, Low humidity, Sick building syndrome, Windy weather[] Inherited GS deficiency Inherited isolated adrenal insufficiency due to CYP11A1 deficiency Inherited zinc deficiency Insensitivity to pain - anhidrosis Insulin-resistance[]

  • Juvenile Paralysis Agitans of Hunt

    Copper deficiency myeloneuropathy may complicate long-term zinc therapy in Wilson’s disease. A similar myeloneuropathy may occur with zinc toxicity.[] alopecia, and nail dystrophy 006857 Frem2 Frem2 ne no eyelid eye, skeleton, coat color, kidney FREM2 Fraser syndrome 003613 Galc Galc twi-5J twitcher 5 Jackson neurological[] Lorain-Levi short stature Necrosis of pituitary gland (postpartum) Panhypopituitarism Pituitary cachexia Pituitary insufficiency NOS Pituitary short stature Sheehan's syndrome[]

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