Knowledge (XXG)

Crandall syndrome

Source 📝

37: 226: 297: 263: 157: 292: 256: 249: 282: 122:
Crandall BF, Samec L, Sparkes RS, Wright SW (1973). "A familial syndrome of deafness, alopecia, and hypogonadism".
58: 101: 287: 204: 151: 78: 70: 139: 233: 131: 36: 74: 135: 276: 66: 62: 54: 225: 143: 199: 77:. It is thought to be an autosomal recessive disorder closely related to 232:
This article about an endocrine, nutritional, or metabolic disease is a
182: 44:
Crandall syndrome is inherited in an autosomal recessive manner
84:
The condition was first reported by B. F. Crandall in 1973.
237: 172: 190: 176: 81:which presents similarly but without hypogonadism. 26: 21: 298:Endocrine, nutritional and metabolic disease stubs 257: 8: 156:: CS1 maint: multiple names: authors list ( 264: 250: 173: 18: 93: 30:Alopecia-deafness-hypogonadism syndrome 149: 57:disorder characterised by progressive 7: 222: 220: 69:demonstrated through low levels of 236:. You can help Knowledge (XXG) by 14: 224: 35: 1: 136:10.1016/s0022-3476(73)80121-0 102:"Orphanet: Crandall syndrome" 61:, hair loss associated with 293:Syndromes affecting hearing 314: 219: 59:sensorineural hearing loss 43: 34: 283:Congenital disorders 71:luteinising hormone 191:External resources 79:Björnstad syndrome 245: 244: 214: 213: 51:Crandall syndrome 48: 47: 22:Crandall syndrome 16:Medical condition 305: 266: 259: 252: 228: 221: 174: 162: 161: 155: 147: 119: 113: 112: 110: 108: 98: 39: 19: 313: 312: 308: 307: 306: 304: 303: 302: 273: 272: 271: 270: 217: 215: 210: 209: 186: 185: 171: 166: 165: 148: 121: 120: 116: 106: 104: 100: 99: 95: 90: 53:is a very rare 17: 12: 11: 5: 311: 309: 301: 300: 295: 290: 288:Rare syndromes 285: 275: 274: 269: 268: 261: 254: 246: 243: 242: 229: 212: 211: 208: 207: 195: 194: 192: 188: 187: 181: 180: 178: 177:Classification 170: 169:External links 167: 164: 163: 114: 92: 91: 89: 86: 75:growth hormone 46: 45: 41: 40: 32: 31: 28: 24: 23: 15: 13: 10: 9: 6: 4: 3: 2: 310: 299: 296: 294: 291: 289: 286: 284: 281: 280: 278: 267: 262: 260: 255: 253: 248: 247: 241: 239: 235: 230: 227: 223: 218: 206: 202: 201: 197: 196: 193: 189: 184: 179: 175: 168: 159: 153: 145: 141: 137: 133: 129: 125: 118: 115: 103: 97: 94: 87: 85: 82: 80: 76: 72: 68: 64: 60: 56: 52: 42: 38: 33: 29: 25: 20: 238:expanding it 231: 216: 198: 152:cite journal 130:(3): 461–5. 127: 123: 117: 105:. Retrieved 96: 83: 67:hypogonadism 50: 49: 107:22 December 27:Other names 277:Categories 88:References 63:pili torti 55:congenital 124:J Pediatr 200:Orphanet 144:4698933 142:  65:, and 234:stub 158:link 140:PMID 109:2016 73:and 205:202 132:doi 279:: 203:: 154:}} 150:{{ 138:. 128:82 126:. 265:e 258:t 251:v 240:. 183:D 160:) 146:. 134:: 111:.

Index


congenital
sensorineural hearing loss
pili torti
hypogonadism
luteinising hormone
growth hormone
Björnstad syndrome
"Orphanet: Crandall syndrome"
doi
10.1016/s0022-3476(73)80121-0
PMID
4698933
cite journal
link
D
Orphanet
202
Stub icon
stub
expanding it
v
t
e
Categories
Congenital disorders
Rare syndromes
Syndromes affecting hearing
Endocrine, nutritional and metabolic disease stubs

Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.